Ultra Rapid Self-contained Biological Indicator for Steam sterilization processes. Geobacillus stearothermophilus (ATCC 7953) 10^6 spores per vial. Readout: 20 minutes. An optional visual pH color change confirmation could be made after 48 hours of incubation. If the sterilization process has not been successful, the culture medium will change to a greenish color first, and then to yellow during incubation at 60 ºC, thus showing the presence of living spores. If the sterilization process is successful culture medium will remain purple after the incubation process. 7-day readout is optional and not intended to be routinely performed; it is an initial validation of the 20 minute-reading. Fluorescence results may be compared to the 7-day visual reading. Note: If 7-day readout is performed, a humidified environment will be required to avoid medium to dry out. D-Value: Not lower than 1.5 minutes at 121 ºC. Another D-value is informed at 132ºC and at 135ºC. Z-Value is informed. Instructions For Use: Identify the Terragene® Bionova® BT224 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT224 SCBI from the sterilized package. (Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature.) 5. Check the Process Indicator on SCBI label. A color change to brown indicates that the SCBI has been exposed to Steam. ( This color change does not evidence the process effectiveness to achieve sterility. If the Process Indicator color has not changed, check the sterilization process.) 6. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. 7. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader Incubators for a maximum of 20 minutes at (60 ± 2) °C for ultra rapid readout. Important: Use a non-sterilized SCBI as a positive control at least once per day, when a sterilization cycle is run. The positive control ensures that correct incubation conditions were met; capability of medium to promote rapid growth; viability of spores has not been altered due to improper storage temperature, humidity or proximity to chemicals and proper functioning of Terragene® Bionova® Auto-Reader Incubators. Both, the positive control indicator and the processed indicator, should belong to the same batch. Note: Holding time between sterilization and incubation should not exceed a 7-day period. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means a failure in the sterilization process. If no fluorescence is detected at 20-minute incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for a visual color change.

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Hyper Rapid Self-contained Biological Indicator for Vaporized Hydrogen Peroxide sterilization processes. Final readout: 5 minutes. Indications For Use: Terragene® Bionova® BT98 fluorescence hyper rapid readout Biological Indicators have been designed for quick and easy monitoring of Plasma or vaporized hydrogen Peroxide sterilization cycles. Device Description: Terragene® Bionova® BT98 fluorescence hyper rapid readout Biological Indicators are single-use Self-Contained Biological Indicators (SCBIs) that consist of a polypropylene tube, a spore carrier and a glass ampoule with a culture medium, enclosed with a colored cap. Each tube contains a population of Geobacillus stearotermophilus ATCC 7953 spores inoculated on a spore carrier, a plastic cap with holes and a barrier permeable to Plasma or Vaporized Hydrogen Peroxide. Each BT98 has a Process Indicator on label that changes from purple to green when exposed to hydrogen peroxide. Precautions: Warning: Do not use Terragene® Bionova® BT98 SCBI to control EO, Dry Heat, Formaldehyde or other sterilization processes different from specified. Do not reuse SCBI. Warning:  Place one or more SCBI in sterilizing hard-to-reach areas to ensure all areas of the chamber are sterilized. Please evaluate all load configurations to ensure ALL hard-to-reach areas have been identified, and place a SCBI in each of those locations. Warning:  Do not reuse the sterilizer until the SCBI test result is negative. Instructions For Use: Identify the Terragene® Bionova® BT98 SCBI by writing the sterilizer number (incase of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. Caution Wear safety glasses and gloves when removing the Terragene® Bionova® BT98 SCBI from the sterilized package. ( Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature.) Check the Process Indicator on SCBI label. A color change to green indicates that the SCBI has been exposed to Hydrogen Peroxide. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the color of the Process Indicator has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® auto-reader incubators for a maximum of 5 minutes at (60 ± 2) °C for hyper rapid readout. (Holding time between sterilization and incubation should not exceed a 1-hour period.) Important: Use a non-sterilized SCBI as a positive control at least once per day, when a sterilization cycle is run. The positive control ensures that correct incubation conditions were met; the capability of the medium to promote rapid growth; viability of spores has not been altered due to improper storage temperature, humidity or proximity to chemicals and proper functioning of Terragene® Bionova® Auto-Reader Incubators. Both, the positive control indicator and the processed indicator, should belong to the same batch. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means failure in the sterilization process. If no fluorescence is detected after 5 minutes of incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for visual color change. Record positive results and discard the SCBIs immediately, as it is indicated below. Hyper Rapid Readout: 5 minutes The hyper rapid readout must be carried out in the appropriate Terragene® Bionova® auto-reader incubators. Fluorescence is emitted after the reader stimulates the spore carrier with UV light. Final readout of negative results is readily available after 5 minutes of incubation. Fluorescence readout is an indirect measure of the viability of Geobacillus stearothermophilus spores after the sterilization process (positive results). Furthermore, a failure in the sterilization process can also become evident by culture medium color-change. Due to the high sensitivity of the fluorescence results at 5 minutes, conventional incubation for color change of Terragene® Bionova® SCBI BT98 is not an advantage. Visual Confirmation: 5 days: Optionally, you can perform a visual color-change confirmation after a 5-day incubation. If the sterilization process has not been successful, culture medium will turn to yellow during incubation at (60 ± 2) ºC, indicating the presence of living spores. If sterilization was successful, culture medium will remain purple after incubation. The positive control must show a color change from purple to yellow for results to be valid. ( If 5-day readout is performed, a humidified environment will be required to prevent medium from drying out.) Readout Time: 7 days A 7-day readout is optional and may be routinely performed. This is an initial validation of the 5-minute readout. Fluorescence results are compared to the 7-day visual readouts. Monitoring Frequency: Follow facility policies and procedures which should specify a biological indicator monitoring frequency compliant with professional association recommended practices and/or national guidelines and standards. As the best practice and to provide optimal patient safety, Terragene® recommends that every sterilization load be monitored with an appropriate biological indicator. Storage: Store in a dark place at temperature between 10-30 ºC and 30-80 % relative humidity. Do not freeze. Do not store biological indicators near sterilizing agents or other chemical products. Shelf Life: Biological Indicators have an expiration date of 2 years from the date of manufacture when stored at recommended conditions. Do not use indicators after their expiration date. Chemical Process Indicator on SCBI label have an expiration date of 2 years when used as part of SCBI. Endpoint Stability Reaction: Chemical Process Indicator endpoint shall remain unchanged for a period of 6 months when stored at previously indicated conditions. Disposal: Discard biological indicators after use according to your country’s healthcare and safety regulations. The positive biological indicators can be autoclaved in a gravity air displacement steam sterilizer at 121 ºC for 5 minutes, 132 ºC for 15 minutes or 134 ºC for 10 minutes; or in a dynamic air removal steam sterilizer at 132 °C for 4 minutes or 135 °C for 3 minutes. Specifications: Population: 10^6 Spores/carrier Read-Out Time: 5 min Regulations: IRAM 37102-1:1999, ISO 11138-1:2017, ISO 13485:2016 / NS-EN ISO 13485:2016

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Rapid Self-contained Biological Indicator for Ethylene Oxide sterilization processes. Bacillus atrophaeus (ATCC 9372) 10^6 spores per vial. Readout: 4 hours. An optional visual pH color change confirmation could be made after 48 hours of incubation. If sterilization process has not been successful, culture medium will change to a greenish color first, and then to yellow during incubation at 37 ºC, thus showing the presence of living spores. If sterilization process is successful culture medium will remain blue after the incubation process. 7-day readout for visual confirmation by color change is optional and not intended to be routinely performed; it is an initial validation of the 4 hour-reading. Fluorescence results may be compared to the 7-day visual reading. Instructions For Use: Identify the Terragene® Bionova® BT110 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT110 SCBI from the sterilized package. Check the Process Indicator on SCBI label. A color change to green indicates that the SCBI has been exposed to Ethylene Oxide. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the color of the Process Indicator has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader incubators for a maximum of 4 hours at (37 ± 2) °C for rapid readout. Note: Holding time between sterilization and incubation should not exceed a 7-day period. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means failure in the sterilization process. If no fluorescence is detected after 4 hours of incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for visual color change. If chamber relative humidity is unknown or < 35 %, continue to incubate the Biological Indicator for a pH color change result, since low relative humidity may increase the fluorescent readout time beyond 4 hours. Specifications: Process: Ethylene Oxide Microorganism: Bacillus atrophaeus (ATCC 9372) Population: 10^6 Spores/carrier Read-Out Time: 4 h Regulations: IRAM 37102-1, IRAM 37102-2, ISO 11138-1, ISO 11138-2 Length: 40 mm

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Super Rapid Self-contained Biological Indicator for Steam sterilization processes. Geobacillus stearothermophilus (ATCC 7953) 10^6 spores per vial. Readout: 1 hour. An optional visual pH color change confirmation could be made after 48 hours of incubation. If sterilization process has not been successful, culture medium will change to a greenish color first, and then to yellow during incubation at 60 ºC, thus showing the presence of living spores. If sterilization process is successful culture medium will remain purple after the incubation process. 7-day readout is optional and not intended to be routinely performed; it is an initial validation of the 1 hour-reading. Fluorescence results may be compared to the 7-day visual reading. Note: if 7-day readout is performed, a humidified environment will be required to avoid medium to dry out. D-Value: Not lower than 1.5 minutes at 121 ºC. Another D-value is informed at 132 ºC and at 135 ºC. Z-Value is informed. Instructions For Use: Identify the Terragene® Bionova® BT222 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT222 SCBI from the sterilized package. WARNING: Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature. Check the Process Indicator on SCBI label. A color change to brown indicates that the SCBI has been exposed to Steam. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the Process Indicator color has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader Incubators for a maximum of 1 hour at (60 ± 2) °C for super rapid readout. Specifications: Process: Steam Microorganism: Geobacillus stearothermophilus (ATCC 7953) Population: 10^6 Spores/carrier Read-Out Time: 1 h Regulations: IRAM 37102-1, IRAM 37102-3, ISO 11138-1, ISO 11138-3

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CDWA4 / Cleaning Indicator for cleaning performance tests. Challenge level: very high. Detects all the factors that affect the result of a washing process. Initial Color: Fuchsia. Result: removal of the fuchsia organic substance. Designed for routine control of cleaning processes and for monitoring automatic washing machines effectiveness as well as monitoring ultrasonic washing machines which operate at frequencies equal to or greater than 35 kHz, and temperatures between 30 ºC and 70 ºC. Characteristics: Challenge Level: Very high. Allows detection of all factors affecting the outcome of cleaning process. Initial Color: Fuchsia. Size: 70 mm x 30 mm (approximate). Synthetic temperature-stable support. Result: Elimination of fuchsia organic substance. To interpret results visually, use the results reference guide on product´s instructions for use. Optionally, the readout of the cleaning indicator can be done using Trazanto Automatic Quality Control and Traceability System (see instructions for use in device´s manual). Instructions For Use: Choose the Chemdye® Splat CDWA indicator according to the desired difficulty. Place the indicator on the Chemdye® Splat CDWAH or Chemdye® Splat CDWAH-U holder. Place the system on the tray along with the material. Once the cleaning cycle is over, remove the indicator. Analyze Chemdye® Splat CDWA indicators using the reference table and record results. If unfavorable results are obtained, perform the appropriate corrective actions and repeat the washing process. Specifications: Process: Cleaning and thermodisinfection Initial Color: Fuchsia Regulations: ISO 13485, ISO/TS 15883-5

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Instructions For Use: Before The Test: Place the holder around the neck of the capsule. Press the holder down so that the groove of the holder fits securely around the neck of the vial. Insert the L shaped end on either side of the holder into the holes of the Ultrasonic device’s basket to hold the vial in position. The holder can be attached to a wire basket or perforated basket. Vials should be placed in the correct location within a tray / basket according to Ultrasonic Cleaning Indicator´s IFU based on the size of the tank. After the test is complete After the ultrasonic cycle remove the vial holding it with three fingers of one hand and the index finger and thumb of the other hand on the holder and lid of capsule. Place the index finger on the end of the holder, then place the thumb on the lid of the capsule for support, push the holder back off the neck of the capsule and remove the holder with both fingers.

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Holder for cleaning and thermodisinfection Indicators. Stainless Steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72 mm long, pin at the back side. ISO/TS 15883-5. Designed to hold Chemdye® CDWA and Integron® IT27W indicators in order to perform routine control of cleaning and thermal disinfection processes in automatic machines. Characteristics: Chrome plating SUS304 grade stainless steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72.5 mm long, pin at the back side. Basket: 32 mm wide, 37 mm long, 0.5 mm thick. The holder is designed to mimic the cleaning challenges posed by a large process load during the washing cycle and can be fixed on the tray, which allows reproducible location of the cleaning indicator in the washer-disinfector. When CDWA4 is placed within the holder, half of the test soil is obscured, thus simulating the joint of a surgical instrument, with water stream hitting it indirectly. The other half of the test soil is covered by a mesh, thus posing a difficulty for water stream to reach it, mimicking shadowed or occluded surfaces. The new design of CDWAH optimizes the control of the washer disinfectors ability to force water and detergent into and onto the test soil. Specifications: Process: Cleaning and thermodisinfection Regulations: ISO 15883

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CDWAH-U / Stainless steel re-usable holder of great resistance and durability. The holder is designed to be fixed on the tray, which allows reproducible location of the cleaning indicator in ultrasonic washing machines. Base: 32,7 mm wide, 72,5 mm long. Designed to hold Chemdye® CDWA cleaning indicators and perform routine control of cleaning processes in ultrasonic washers. Characteristics: Chrome plating SUS304 grade stainless steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72.5 mm long, pin at the back side. The holder is designed to be fixed on the tray, which allows reproducible location of the cleaning indicator in ultrasonic washing machines, without representing a challenge to the washing process. Specifications: Process: Cleaning and thermodisinfection Regulations: ISO/TS 15883-5

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IT26-1YS / Unique point chemical integrator for Steam sterilization processes between 121° C and 134° C. Control of Steam sterilization processes between 121 ºC and 135 ºC. Characteristics: Type 5 Integrator Indicator (according to ISO 11140-1). One-side-laminated strips printed with indicator ink. Size: 70 mm x 23 mm. Initial Color: Yellow. Final Color: Black. 100 % Toxic Heavy Metal free. Instructions For Use: Place a chemical integrator Integron® IT26-1YS within each package, bag or tray that will be sterilized by Steam. In rigid containers place an IT26-1YS in every corner, or at least two diagonally opposite corners, to ensure that steam has reached the most inaccessible areas. Perform the sterilization cycle. After the sterilization process has finished, remove the indicators from the sterilizer and analyze the results. For all the chemical indicators exposed to Steam, the ink must turn to the black reference color when the integration conditions are reached. Specifications: Process: Steam Initial Color: Yellow Final Color: Black Indicator Type: Type 5 chemical indicator Regulations: ISO 11140-1 More Info About This Product: Color Chart

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2 level chemical integrator for Ethylene Oxide sterilization processes. One-side laminated strips. Metals free. Integron® IT12 Chemical Integrators (Type 5 according to ISO 11140-1:2014 standard) are single-use two level chemical indicators that consist of paper strips laminated on the back side and printed with indicator ink. They have been designed for monitoring Ethylene Oxide (EO) sterilization processes. The integration level contains a purple/brown ink which was developed to turn to green when a theoretical spore population reaches its kill time, thus indicating that the SAFE condition has been met. Level 1 – Red: Exposure level. Indicator ink turns yellow to indicate exposition to the process, but does not ensure that the variables required to achieve the integration condition have been achieved (UNSAFE condition). Level 2 – Purple / brown: Integration level. Indicator ink turns green to indicate that the integration condition indicated in the quality certificate has been achieved. This condition consists of the kill time of a theoretical 106 Bacillus atrophaeus spore population, calculated in a BIER (Biological Indicator Evaluator Resistometer), and is called SAFE condition. Indicators 100% free of toxic heavy metals. Instructions For Use: Place a Integron® IT12 Chemical Integrator along with the material to be sterilized in a suitable package according to the recommended sterilization techniques. Place the indicators in those areas of most difficult access to the sterilizing agent. Perform the sterilization cycle. After the sterilization process has finished and evacuation/ventilation process is over, you may:               A. Remove the integrator indicator taking the necessary precaution to avoid                          contact with the remaining sterilizing agent.              B. Ventilate the load together with the integrator indicator and then perform                        the reading. Analyze the results. If the SAFE integration condition has been reached, the        sterilization process has been effective. Specifications: Process: Ethylene Oxide Initial Color: Level 1 Red, Level 2 purple-brown Final Color: Level 1 Yellow, level 2 Green Indicator Type: Type 5 chemical indicator Regulations: ISO 11140-1 More Info About This Product: Color Chart

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IT26-C Extender/ Moving front Chemical Integrator to monitor Steam sterilization processes between 118°C and 138°C. Control of Steam sterilization processes between 118 °C and 138 °C. Characteristics: Type 5 Integrating Indicator (according to ISO 11140-1). Size: 52 mm x 21 mm. Chemical Integrator consists of a paper wick and a steam and temperature sensitive chemical pellet contained in a paper/film/foil laminate. The chemical pellet melts and migrates as a dark bar along the paper wick. The migration is visible through a zone marked ACCEPT or REJECT, thus indicating whether sterilization conditions were met. The extent of migration depends on steam quality, time, and temperature. The ACCEPT result is reached when a theoretical spore population reaches its kill time, indicating integration condition has been reached. This condition is calibrated with the kill time of 106 Geobacillus stearothermophilus spore population, calculated in BIER (Biological Indicator Evaluator Resistometer). Conditions: saturated steam at 121 °C, 128 °C, 135 °C. Optionally, the readout of the chemical indicator can be done using Trazanto Automatic Quality Control and Traceability System (see instructions for use in device´s manual). Instructions For Use: Carefully open the package and remove only the number of indicators needed. Reseal the package tightly. Place a Integron® IT26-C indicator in each pack, peel pouch, container system or tray to be steam sterilized in the most inaccessible area to sterilizing agent. Perform de sterilization cycle. 4After the sterilization process has finished, the dark bar should have reached the ACCEPT zone. If the dark bar has not reached the ACCEPT zone, a REJECT result is indicated and the items in the pack, peel pouch, container system, or tray were not exposed to proper steam sterilization conditions. These items should be reprocessed according to established procedures and a new IT26-C has to be used. NOTE: In some extended or wet steam cycles, the dark bar can display discoloration in some zones of the reading window, imposing a difficulty for result´s interpretation (see Result Reference Guide for reference). Despite this, regarding cycle integration parameters, this process can be considered as accepted. In case the IT26-C indicator shows a damp appearance after the sterilization process, Terragene® recommend planning an equipment´s maintenance.

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IT26-C / Moving front Chemical Integrator to monitor Steam sterilization processes between 118°C and 138°C. Control of Steam sterilization processes between 118 °C and 138 °C. Characteristics: Type 5 Integrating Indicator (according to ISO 11140-1). Size: 52 mm x 21 mm. Chemical Integrator consists of a paper wick and a steam and temperature sensitive chemical pellet contained in a paper/film/foil laminate. The chemical pellet melts and migrates as a dark bar along the paper wick. The migration is visible through a zone marked ACCEPT or REJECT, thus indicating whether sterilization conditions were met. The extent of migration depends on steam quality, time, and temperature. The ACCEPT result is reached when a theoretical spore population reaches its kill time, indicating integration condition has been reached. This condition is calibrated with the kill time of 106 Geobacillus stearothermophilus spore population, calculated in BIER (Biological Indicator Evaluator Resistometer). Conditions: saturated steam at 121 °C, 128 °C, 135 °C. Optionally, the readout of the chemical indicator can be done using Trazanto Automatic Quality Control and Traceability System (see instructions for use in device´s manual). Instructions For Use: Carefully open the package and remove only the number of indicators needed. Reseal the package tightly. Place a Integron® IT26-C indicator in each pack, peel pouch, container system or tray to be steam sterilized in the most inaccessible area to sterilizing agent. Perform de sterilization cycle. After the sterilization process has finished, the dark bar should have reached the ACCEPT zone. If the dark bar has not reached the ACCEPT zone, a REJECT result is indicated and the items in the pack, peel pouch, container system, or tray were not exposed to proper steam sterilization conditions. These items should be reprocessed according to established procedures and a new IT26-C has to be used. Despite this, regarding cycle integration parameters, this process can be considered as accepted. In case the IT26-C indicator shows a damp appearance after the sterilization process, Terragene® recommend planning an equipment´s maintenance. Specifications: Process: Steam Indicator Type: Type 5 chemical indicator Regulations: ISO 11140-1 More Info About This Product: User Manual

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CD40 / Multi-variable Chemical Indicator, strips printed with reactive ink for Plasma or Vaporized Hydrogen Peroxide sterilization processes. Control of plasma or vaporized H2O2 sterilization processes. Conditions: 6 minutes, 50 °C, 2,3 mg/l H2O2. Characteristics: Type 4 Chemical Indicator (according to ISO 11140-1). Strips printed with indicator ink. Size: 105 x 18 mm (approximate). Initial color: Purple. Final color: Green. 100 % Toxic Heavy Metals free. Instructions For Use: Place a Chemdye® CD40 Multivariable Process Indicator within each package, bag or tray that will be sterilized by Plasma or Vaporized Hydrogen Peroxide. In rigid containers, place the indicator in every corner, or at least two diagonally opposite corners, to ensure that the sterilization agent has reached the most inaccessible areas. Perform the sterilization cycle. After the sterilization process has finished, remove the indicators from the sterilizer and analyze the results. For all the chemical indicators exposed to Plasma or Vaporized Hydrogen Peroxide, the ink must turn to the green or lighter reference color when the sterilization parameters are reached. Specifications: Process: Hydrogen peroxide Initial Color: Purple Final Color: Green Indicator Type: Type 4 chemical indicator Regulations: ISO 11140-1 More Info About This Product: Color Chart

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Chemical Indicator, strips printed with reactive ink for Plasma or Vaporized Hydrogen Peroxide sterilization processes.Internal Control. Metals Free. Chemdye® CD42 Process Indicators (Type 1 according to ISO 11140-1:2014 standard) are single-use chemical indicators that consist of plastic strips printed with indicator ink. These indicators have been designed to monitor Plasma or Vaporized Hydrogen Peroxide sterilization processes within loads, ensuring an adequate exposure to the sterilizing agent during the sterilization process and allowing to distinguish between processed and unprocessed items. Innovative highly sensitive red ink was developed to turn to yellow when the indicator is exposed to Plasma or Vaporized Hydrogen Peroxide. Endpoint condition: 50 ºC, 6 minutes, 2.3 mg/l H2O2. Indicators 100% free of toxic heavy metals. Instructions For Use: Place a Chemdye® CD42 Process Indicator within each package, bag or tray that will be sterilized by Plasma or Vaporized Hydrogen Peroxide. In rigid containers, place the indicator in every corner, or at least two diagonally opposite corners, to ensure that the sterilization agent has reached the most inaccessible areas. Perform the sterilization cycle. After the sterilization process has finished, remove the indicators from the sterilizer and analyze the results. For all the chemical indicators exposed to Plasma or Vaporized Hydrogen Peroxide, the ink must turn to the yellow reference color when the sterilization parameters are reached. For reference color, please refer to Result Reference Guide. More Info About This Product: Color Chart

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Proprietary TotalClean™ technology provides 1-step cleaning and disinfection in a best-in-class contact time of just 1 minute. Eliminates 48 pathogens, including bacteria, fungi, TB and viruses, including the coronavirus, without damaging surfaces. Ideal for large, non-porous surfaces. ProSurface Disinfectant Spray, Eliminates 48 pathogens, including bacteria, fungi, TB and viruses, including the coronavirus, without damaging surfaces. *Treated surface must remain visibly wet for one minute. Active ingredients: ethyl alcohol 72.5% and didecyl dimethyl ammonium chloride 0.33 Pro-Surface disinfectant spray, 32 oz bottle

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Proprietary TotalClean technology provides 1-step cleaning and disinfection in a best-in-class contact time of just 1 minute. Eliminates 48 pathogens, including bacteria, fungi, TB and viruses, including the coronavirus, without damaging surfaces.

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Proprietary TotalClean technology provides 1-step cleaning and disinfection in a best-in-class contact time of just 1 minute. Eliminates 48 pathogens, including bacteria, fungi, TB and viruses, including the coronavirus, without damaging surfaces.

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Versatile all-purpose glove made with the unrivaled strength and durability of nitrile to deliver enhanced barrier protection and exceptional fit. Textured fingertips ensure a secure grip, even when wet. Chemo-tested SafeBasics True Fit Thin Powder-Free Nitrile Gloves, Blue. Small. 300/bx, 8 bx/cs

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SafeSeal® Quattro sterilization pouches are made from high quality porous medical paper and mechanically sealed with TruePress™ technology. The perforated fold facilitates precise folding of a wide self-adhesive strip to form an airtight seal. Internal and external multiparameter process indicators for steam sterilization respond to three variables: time, temperature and saturated steam. The multiparameter process indicators printed directly on the pouch confirm sterilization parameters. Blue-tinted film makes it easy to view instruments and detect punctures or tears. Convenient thumb notch makes it easy to open the pouch without contaminating the contents.

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SafeSeal® Quattro sterilization pouches are made from high quality porous medical paper and mechanically sealed with TruePress™ technology. The perforated fold facilitates precise folding of a wide self-adhesive strip to form an airtight seal. Internal and external multiparameter process indicators for steam sterilization respond to three variables: time, temperature and saturated steam. The multiparameter process indicators printed directly on the pouch confirm sterilization parameters. Blue-tinted film makes it easy to view instruments and detect punctures or tears. Convenient thumb notch makes it easy to open the pouch without contaminating the contents.

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SafeSeal® Quattro sterilization pouches are made from high quality porous medical paper and mechanically sealed with TruePress™ technology. The perforated fold facilitates precise folding of a wide self-adhesive strip to form an airtight seal. Internal and external multiparameter process indicators for steam sterilization respond to three variables: time, temperature and saturated steam. The multiparameter process indicators printed directly on the pouch confirm sterilization parameters. Blue-tinted film makes it easy to view instruments and detect punctures or tears. Convenient thumb notch makes it easy to open the pouch without contaminating the contents.

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Cleans instruments, burs and apparatus. Removes blood, bioburden, contaminants and more. Also removes buffing compounds in a lab setting. Packed in super concentrated 1 oz tubes. 1 oz makes 1 gallon of cleaning solution. For use in an ultrasonic cleaner. Concentrated, 128:1 dilution ratio Single dose application Super convenient and easy to use Removes blood and organic debris from instruments and apparatus Can also be used as a carrier bath Product Attachments: Material Safety Dats Saheet

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Powder based product that cleans dentures, partials and bridges. Add one packet to 6 oz of water in a beaker and insert denture. Use one packet per cleaning. Discard solution after. For use in an ultrasonic cleaner. Concentrated Powder formula Single dose application Super convenient and easy to use Cost effective Eliminates spills and mess Application:  Cleans dentures, partials and bridges when used with a beaker or plastic bag in an ultrasonic cleaning machine. Product Attachments: Material Safety Data Sheet

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Safe for use on non-porous surfaces. Effective against TB in 3 minutes, and HIV-1, HCV, HBV and MRSA in 2 minutes. Disinfectant, cleaner, decontaminant, all in one. May be used on most medical device materials. For use on hard, non-porous surfaces. Ideal for hospitals, medical/dental offices, daycares, schools, clean rooms, home sanitizing, and nursing facilities CaviCide Disinfectant kills the following viruses within minutes. Mycobacterium tuberculosis var: bovis (BCG) (TB) Staphylococcus aureus Pseudomonas aeruginosa Salmonella enterica Trichophyton mentagrophytes Resistant Staphylococcus aureus (MRSA) Vancomycin Resistant Enterococcus faecalis (VRE) Staphylococcus aureus with reduced susceptibility to vancomycin Hepatitis B Virus (HBV) Hepatitis C Virus (HCV) Herpes Simplex Virus Types 1 and 2 Human Immunodeficiency Virus (HIV-1) Human Coronavirus (not associated with Severe Acute Respiratory Syndrome or SARS) Influenza A2 Virus Features This product may be used in healthcare settings such as: Hospitals Operating rooms Emergency medical settings Surgical centers Outpatient Surgical Centers Isolation areas Neonatal units Laboratories Nursing homes Ophthalmic and optometric facilities Dental offices Animal care facilities Salon settings Emergency vehicles Schools Health club facilities Bathrooms Daycare centers Correctional facilities Laundry rooms Other critical care areas where control of cross contamination between treated surfaces is important. It also effectively clean and disinfect, when used as directed, such items: Interior and exterior surfaces of infant incubators, bassinets Infant/child care equipment surfaces Oxygen hoods Ambulance equipment surfaces Amalgamators and dental curing lights Exterior surfaces of anesthesia machines and respiratory therapy equipment This product is not to be used as a terminal sterilant/high level disinfectant on any surface or instrument that (1) is introduced directly into the human body, either into or in contact with the bloodstream or normally sterile areas of the body, or (2) contacts intact mucous membranes but which does not ordinarily penetrate the blood barrier or otherwise enter normally sterile areas of the body. This product may be used to preclean or decontaminate critical or semi-critical medical devices prior to sterilization or high level disinfection. This product may be used to disinfect non-critical medical devices, which come in contact only with intact skin. Manufacturer # 13-1025 Brand CaviCide™ Manufacturer Metrex Research Active Ingredients Isopropyl Alcohol Application Surface Disinfectant Cleaner Container Type Jug Dispensing Method Manual Pour Form Liquid Scent Alcohol Scent Sterility NonSterile Type Alcohol Based UNSPSC Code 42281604 Volume 2.5 gal.

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Advanced Sterilization Pouch: Elevate Your Sterilization Procedures Introducing our Sterilization Pouch, sized 10" x 15", a must-have for every medical and dental facility. With a focus on convenience, efficiency, and compliance, this product is designed to elevate your sterilization processes.What sets our pouch apart is its unique peel-off indicator that ensures thorough heat penetration within the pouch. Bid farewell to purchase secondary indicator strips – our pouch is a self-sufficient solution. It conveniently affixes to patient files, creating a permanent sterilization record, and aligning with CDC requirements for internal indicators.Crafted to the highest standards, our pouch boasts dual external heat and gas sterilization indicators, providing double assurance of successful sterilization. Certified for a remarkable minimum 5-year post-sterilization lifespan, it guarantees prolonged reliability.The aqua-tinted, transparent four-ply film allows easy identification of instrument setups, enabling swift recognition of compromised sterility. Coupled with medical-grade paper, this pouch enables optimal steam and gas penetration. Quality seals bolster its strength while ensuring a clean, fiber-free peel.

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Revolutionize Sterilization with Our State-of-the-Art 11" x 16" Sterilization Pouch: Unmatched Quality and Innovation Introducing our Sterilization Pouch, 11" x 16", a pinnacle of innovation and reliability for your sterilization needs. With a unique peel-off indicator, this pouch takes the guesswork out of sterilization. The indicator confirms heat penetration within the pouch, eliminating the need for secondary indicator strips. It seamlessly affixes to the patient file, ensuring a permanent record of the sterilization process.Meeting CDC requirements, our pouch features dual external heat and gas sterilization indicators. The certification for a minimum 5-year post-sterilization life underscores its longevity. The aqua-tinted, see-through, four-ply film enables swift instrument identification and allows for immediate assessment of sterility. Crafted from medical-grade paper, it enables thorough steam and gas penetration.Our pouch boasts quality seals that not only enhance its durability but also guarantee a clean, fiber-free peel. The easy-to-open overlap design streamlines your workflow. With a wide range of sizes tailored to various indications, it accommodates your diverse needs.Trust in a product that combines cutting-edge features, uncompromising quality, and adherence to the highest standards. Elevate your sterilization practices with our advanced pouch – an assurance of safety, efficiency, and peace of mind.

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Unparalleled Sterilization Confidence: Introducing our 12" x 18" Sterilization Pouch with Innovative Peel-Off Indicator Introducing our Sterilization Pouch, sized at 12" x 18", available in a convenient pack of 100. Designed to revolutionize your sterilization process, this pouch boasts a unique peel-off indicator that eliminates the need for separate indicator strips. Watch with confidence as the indicator confirms thorough heat penetration within the pouch, ensuring optimal sterilization without compromise.Crafted to meet CDC requirements, this pouch features an internal indicator for each package, streamlining your compliance process. The innovative dual external heat and gas sterilization indicators further reinforce its reliability. With a certified minimum 5-year post-sterilization life, rest assured that your instruments remain impeccably sterilized until use.Its aqua-tinted, four-ply film allows for effortless identification of instrument setups while safeguarding sterility. The robust medical-grade paper facilitates seamless steam and gas penetration. Quality seals augment the pouch's strength and offer a pristine, fiber-free peel every time.The pouch's user-friendly overlap design ensures easy opening, saving crucial moments in critical situations. With a range of sizes catering to diverse needs, this sterilization pouch stands as the pinnacle of safety and convenience. Elevate your sterilization procedures and uphold the highest standards of quality with this exceptional solution.

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Advanced Sterilization Pouch: Confidence in Protection and Precision Introducing our Sterilization Pouch, sized at 2¼" x 4", a true game-changer for your medical and dental sterilization needs. This remarkable product boasts a unique peel-off indicator, eliminating the necessity for additional indicator strips. With this innovation, you can effortlessly confirm heat penetration within the pouch, ensuring impeccable sterilization.Crafted to meet the rigorous demands of healthcare facilities, this pouch firmly adheres to patient files, creating an enduring record of sterilization procedures. Complying with CDC mandates, it integrates an internal indicator, guaranteeing precision in each package.Equipped with dual external heat and gas sterilization indicators, this pouch is your steadfast partner in upholding safety standards. Its certification for a minimum 5-year post-sterilization lifespan showcases its durability and reliability.Crafted with an aqua-tinted, transparent four-ply film, the pouch allows easy identification of instrument setups while offering a quick assessment of sterility status. Its robust, medical-grade paper ensures thorough steam and gas penetration, while quality seals amplify strength and a pristine, fiber-free peel.

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"Innovative Sterilization Pouch: Streamlined Confidence for Your Sterilization Process" Introducing our Sterilization Pouch, sized at 2¾" x 10", available in a convenient pack of 200. Revolutionize your sterilization process with this advanced solution that ensures the utmost confidence and convenience.Designed with precision, this pouch boasts a unique peel-off indicator, eliminating the need for separate indicator strips. Watch as it transforms, confirming thorough heat penetration within the pouch during sterilization cycles. This innovation aligns with CDC requirements, eliminating the guesswork and streamlining your process.Crafted for excellence, our pouch affixes effortlessly to patient files, offering a permanent sterilization record. The inclusion of dual external heat and gas sterilization indicators guarantees accuracy, while its remarkable certification for a minimum 5-year post-sterilization lifespan promises longevity.Through its aqua-tinted, four-ply film, you can effortlessly assess instrument setups and detect any compromise in sterility. The medical-grade paper, designed for steam and gas penetration, ensures robust performance. Quality seals reinforce strength, culminating in a fiber-free peel through the easy-to-open overlap design.

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"Innovative Sterilization Confidence: Introducing our Advanced 3¼" x 6½" Sterilization Pouch - 200/bx" Introducing our Sterilization Pouch, sized at 3¼" x 6½", available in a convenient pack of 200. Designed with meticulous attention to detail, this pouch is a paramount addition to your medical facility or dental practice.Crafted with innovation in mind, this pouch features a unique peel-off indicator that revolutionizes the sterilization process. With its smart design, it ensures absolute heat penetration within the pouch, eliminating the need for secondary indicator strips. Furthermore, this indicator conveniently adheres to the patient's file, creating a permanent record of the sterilization process, and fostering accountability and compliance.Exceeding the stringent standards set by the CDC, our pouch includes dual external heat and gas sterilization indicators, offering an added layer of assurance. Certified for a remarkable minimum 5-year post-sterilization life, this product is synonymous with reliability.The aqua-tinted, see-through four-ply film empowers you to effortlessly inspect instrument setups while also facilitating the identification of any potential compromise in sterility. Its robust medical-grade paper allows seamless steam and gas penetration, while the quality seals augment strength and deliver a clean, fiber-free peel.

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Advanced Sterilization Pouch: Ensuring Unrivaled Safety and Convenience Introducing our Sterilization Pouch, sized perfectly at 3½" x 10", offering exceptional sterilization assurance and convenience. With its ingenious peel-off indicator, your worries about heat penetration are put to rest. This unique feature eliminates the need for purchasing additional indicator strips, saving you time and resources.Designed to streamline record-keeping, the peel-off indicator can be affixed to the patient's file, providing a permanent record of the sterilization process. Meeting CDC requirements, the pouch boasts dual external heat and gas sterilization indicators, ensuring the highest level of safety.What sets this pouch apart is its post-sterilization longevity, certified for a remarkable minimum 5-year lifespan. The aqua-tinted, transparent four-ply film grants you visibility into instrument setups while allowing you to swiftly identify any potential compromise in sterility.Crafted from robust, medical-grade paper, this pouch enables thorough steam and gas penetration, while quality seals enhance its strength, ensuring a clean, fiber-free peel. The user-friendly overlap design guarantees easy opening, saving you precious time in critical moments.

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Unparalleled Sterilization Confidence: Introducing our Innovative 5¼" x 7½" Sterilization Pouch Introducing our Sterilization Pouch, 5¼" x 7½", the ultimate solution for your medical sterilization needs. With unique features that set it apart, this product ensures the highest level of safety and convenience.The standout feature is the innovative peel-off indicator that confirms thorough heat penetration within the pouch. No more need for separate indicator strips – this pouch is an all-in-one solution. The indicator also affixes to patient files, providing a permanent sterilization record as per CDC requirements.Crafted to perfection, our pouch boasts dual external heat and gas sterilization indicators, guaranteeing the utmost reliability. It's certified for a remarkable minimum 5-year post-sterilization life, assuring longevity and peace of mind.The aqua-tinted, four-ply film offers transparency, allowing you to easily identify instrument setups and assess sterility without compromising it. The medical-grade paper enables optimal steam and gas penetration while maintaining strength.Enhanced by quality seals for added durability and a clean, fiber-free peel, the easy-to-open overlap design ensures effortless usability. Available in a wide range of sizes, our Sterilization Pouch caters to all indications, making it an indispensable asset for various medical settings.

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Premium Sterilization Pouch: Ensuring Uncompromised Healthcare Safety Introducing our Sterilization Pouch, sized at 5½" x 13", available in a convenient pack of 200. This innovative pouch is meticulously crafted to meet the stringent demands of modern healthcare facilities.Designed with efficiency and reliability in mind, this pouch boasts a unique peel-off indicator that provides instant confirmation of optimal heat penetration within. Bid farewell to the need for secondary indicator strips, as this pouch eliminates that requirement. Moreover, it effortlessly affixes to patient files, ensuring a permanent sterilization record.Meeting CDC standards, this pouch features dual external heat and gas sterilization indicators. Its exceptional certification guarantees a minimum 5-year post-sterilization lifespan, contributing to long-term operational excellence. The aqua-tinted, see-through, four-ply film empowers users to identify instrument setups and gauge sterility status at a glance.Crafted from robust medical-grade paper, this pouch enables seamless steam and gas penetration while maintaining its structural integrity. The quality seals further reinforce its strength, ensuring a clean, fiber-free peel every time. The easy-to-open overlap design streamlines process while the wide range of available sizes caters to diverse needs.Upgrade your sterilization practices with confidence using this advanced pouch. It's not just a pouch; it's a testament to uncompromising quality, lasting performance, and unwavering dedication to safety in healthcare settings.

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Premium Sterilization Pouch: Unmatched Safety and Convenience for Medical Practices Introducing our Sterilization Pouch, 7" x 13", a reliable solution for maintaining impeccable sterilization standards in medical and dental settings. With its cutting-edge features and adherence to stringent guidelines, this pouch guarantees the safety of your instruments and peace of mind for your practice.The standout feature of this pouch is its unique peel-off indicator that revolutionizes the sterilization process. Say goodbye to purchasing secondary indicator strips – our pouch includes a built-in indicator that confirms optimal heat penetration within the pouch. This not only saves you time and resources but also ensures foolproof sterilization without compromise.Designed to meet CDC requirements, our pouch affixes effortlessly to patient files, creating a permanent record of the sterilization process. Dual external heat and gas sterilization indicators provide an extra layer of confidence.Crafted from a strong, medical-grade paper that allows seamless steam and gas penetration, and coupled with quality seals for enhanced strength, these pouches boast a clean, fiber-free peel. The easy-to-open overlap design streamlines the workflow, while the aqua-tinted, see-through, four-ply film allows instant identification of instrument setups and assessment of sterility status.

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Help your family and those you care for, kill germs on their hands. You don't want to think about it, but it's true that illness-causing germs are everywhere at home at work and when you're out and about. We know that life moves fast and that washing your hands with soap and water is not always an option. Using it on multiple occasions throughout the day conveniently helps eliminate germs on your hands. These pre-moistened wipes are soft textured and durable to gently clean up hands or faces. They are also dermatologist tested, providing safe and effective cleaning when soap and water are not available. These individually wrapped hand wipes fit just about anywhere. Put it in your pocket or bag. Add to boxed lunches or meal trays, as a caring touch. Formulated to be gentle on the skin. The case includes 300 individually wrapped. GOJO Industries, a purpose-driven Family Enterprise, invented the PURELL brand 30 years ago. Our team is committed to using the best science available to make the world a better place. Free of harsh preservatives Do not contain dye, triclosan, parabens or phthalates They are a simple amenity to show you care. Using PURELL wipes is a convenient and gentle way to kill germs and stay healthy Proven to kill 99.99% of most common germs that may cause illness without damaging the skin Manufacturer # 9022-10 Brand Purell® Manufacturer GOJO Country of Origin United States Active Ingredients Ethyl Alcohol Application Hand Sanitizing Wipe Container Type Individual Packet Form Wipe Product Dating McKesson Acceptable Dating: we will ship >= 90 days Scent Alcohol Scent Strength 62% Strength UNSPSC Code 53131626 Volume 100 Count

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Premium Sterilization Pouches: Safeguarding Hygiene for Your Practice Introducing our Sterilization Pouch, designed to ensure the utmost safety and hygiene in your medical or dental practice. With dimensions of 7½" x 13", these pouches provide ample space to accommodate a variety of medical instruments while maintaining their sterile integrity.Each box contains 200 pouches, offering an efficient solution to your sterilization needs. Our pouches are constructed using high-quality, medical-grade materials that effectively seal and protect your instruments from contaminants, ensuring they remain in a pristine condition until they're ready for use. The transparent front surface allows easy visibility, enabling quick instrument identification without compromising the sterilized environment.These pouches are equipped with an easy-to-use self-sealing adhesive strip, eliminating the need for additional equipment or heat sealing. Whether you're running a bustling hospital or a small clinic, our sterilization pouches provide the reliability and convenience you require.Prioritize the safety of your patients and the integrity of your practice with our dependable Sterilization Pouches. With 200 pouches per box, you're making a lasting investment in maintaining a sterile environment for your valuable instruments. Trust in our product to deliver impeccable results, every time.

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Formulated with moisturizers for the skin, this lotion removes 3M™ DuraPrep™ Surgical Solution (Iodine Povacrylex [0.7% available iodine] and Isopropyl Alcohol, 74% w/w) Patient Preoperative Skin Preparation Removes iodophor color, tincture of benzoin, prep film and other materials soluble in alcohol Wipes away quickly and easily in as little as 25 seconds Does not compromise tape or dressing adhesion Contains non-irritating and fragrance-free skin softeners and a moisturizer More Information SDS Manufacturer # 8611 Brand 3M™ Manufacturer 3M Country of Origin United States Application Remover Lotion Container Type Squeeze Bottle Form Liquid NDC Number 08333861101 UNSPSC Code 42311551 Volume 4 oz. Latex Free Indicator Not Made with Natural Rubber Latex

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The easy, gentle and effective way to remove 3M™ DuraPrep™ Surgical Prepping Solution Removes iodophor color, tincture of benzoin, prep film and other materials soluble in alcohol No scrubbing necessary Does not compromise tape or dressing adhesion Contains non-irritating and fragrance-free skin softeners and a moisturizer More Information SDS Manufacturer # 8610 Brand 3M™ Manufacturer 3M Country of Origin Turkey Application Lotion Remover Container Type Individual Packet Form Liquid NDC Number 08333861001 UNSPSC Code 42311551 Volume .5 oz. Latex Free Indicator Not Made with Natural Rubber Latex

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3M™ Tegaderm™ Transparent Film Dressings can be used to cover and protect catheter sites and wounds, to maintain a moist environment for wound healing, and to secure devices to the skin Provides a waterproof, sterile barrier to external contaminants including liquids, bacteria and viruses Gentle to the skin, yet holds catheters and other devices in place Hypoallergenic Dressing is conformable and flexes with skin for greater patient comfort Unique shapes and designs for both I.V. and wound needs More Information SDS Manufacturer # 1626 Brand 3M™ Tegaderm™ Manufacturer 3M Country of Origin United States Application Transparent Film Dressing Delivery Method Frame Style Delivery Dimensions 4 X 4-3/4 Inch Label Without Label Length Up to 4 Inch Length Material Adhesive / Film NDC Number 08333162601 Shape Rectangle Shape Range Rectangle / Sqaure Sterility Sterile UNSPSC Code 42311527 Width 4 Inch Width Latex Free Indicator Not Made with Natural Rubber Latex

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3M Tegaderm Transparent Film Dressings can be used to cover and protect catheter sites and wounds, to maintain a moist environment for wound healing, and to secure devices to the skin Provides a waterproof, sterile barrier to external contaminants including liquids, bacteria and viruses Gentle to the skin, yet holds catheters and other devices in place Hypoallergenic Picture-frame delivery makes accurate placement easy Stretch and release removal prevents skin irritation Unique shapes and designs for both I.V. and wound needs Manufacturer # 1626W Brand 3M™ Tegaderm™ Manufacturer 3M Country of Origin Phillippines Application Transparent Film Dressing Delivery Method Frame Style Delivery Dimensions 4 X 4-3/4 Inch HCPCS A6258 Label With Label Length Up to 4 Inch Length Material Adhesive / Film NDC Number 08333162605 Shape Rectangle Shape Range Rectangle / Sqaure Sterility Sterile UNSPSC Code 42311527 Width 4 Inch Width Latex Free Indicator Not Made with Natural Rubber Latex

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Unique multi-layer design absorbs and evaporates moisture while allowing exudate to pass through to help maintain a moist wound environment that supports healing Fluid management properties of the dressing prevent pooling or migration, which helps reduce the potential for skin maceration Strong and gentle adhesive minimizes disruption to skin during removal Secure with elastic or cohesive wrap, tape or other methods as needed Suitable for use on fragile skin and with compression therapy Strong and gentle adhesive minimizes disruption to skin during removal More Information SDS Manufacturer # 90631 Brand 3M™ Tegaderm™ Manufacturer 3M Country of Origin United States Adhesive Type Silicone Face Application Foam Dressing Backing Material Film Backing Border Type Without Border Color Tan Dimensions 4 X 4-1/4 Inch HCPCS A6210 Length Up to 4 Inch Length Material Foam Shape Square Shape Range Rectangle / Square Sterility Sterile UNSPSC Code 42311510 Width 4 Inch Width

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3M™ Tegaderm™ High Integrity Alginate Dressing helps to maintain a moist wound healing environment for medium to heavily exuding wounds Conformable- Gel forming dressing primary dressing Supports healing – Maintains optimal moisture levels needed for healing tissue. Absorbent- For use on medium to high exuding wounds Compatible with 3M cover dressings More Information SDS Manufacturer # 90120 Brand 3M™ Tegaderm™ High Integrity Manufacturer 3M Country of Origin United Kingdom Application Alginate Dressing Color White Dimensions 12 Inch Length HCPCS A6199 Length 5 to 12 Inch Length Material Calcium Alginate NDC Number 08333901200 Shape Rope Sterility Sterile UNSPSC Code 42311540 Width 9 to 15 Inch Width Latex Free Indicator Not Made with Natural Rubber Latex

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3M™ Tegaderm™ High Gelling Alginate Dressing helps to maintain a moist wound healing environment for medium to heavily exuding wounds. Highly Conformable- Gel forming dressing primary dressing Supports healing – Maintains optimal moisture levels needed for healing tissue Compatible with 3M cover dressings More Information SDS Manufacturer # 90212 Brand 3M™ Tegaderm™ High Gelling Manufacturer 3M Country of Origin United Kingdom Application Alginate Dressing Color White Dimensions 4 X 4 Inch HCPCS A6196 Length Up to 4 Inch Length Material Calcium Alginate NDC Number 08333902120 Shape Square Sterility Sterile UNSPSC Code 42311540 Width 4 Inch Width Latex Free Indicator Not Made with Natural Rubber Latex

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A highly absorbent, antimicrobial wound dressing with an ionic silver complex to fight and prevent infection Effective up to 14 days Antimicrobial Barrier- ionic silver complex is released, protecting the wound from a broad spectrum of microorganisms, including antibiotic-resistant bacteria like MRSA and VRE Comformable - soft-gelling absorbency allows for conformity to wounds, providing soft wound protection for increased comfort for the patient Promotes healing - offers a moist environment to help facilitate moist wound healing Reduces dressing changes - Effective for 14 days, providing for increased patient safety and comfort Versatile - ideal for a variety of wounds that are at increased risk of infection Manufacturer # 90303 Brand 3M™ Tegaderm™ Alginate Ag Manufacturer 3M Country of Origin United Kingdom Application Silver Alginate Dressing Color White Dimensions 4 X 5 Inch Impregnated Ingredients Silver Material Carboxymethyl Cellulose (CMC) / Alginate Shape Rectangle Sterility Sterile Type Non-adhesive Without Border UNSPSC Code 42311540 Volume 10 Count

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3M™ Microfoam™ Surgical Tape offers a conformable elastic foam tape that stretches for compression applications or securing dressings on challenging areas Conforms readily; water resistant Secure adhesion to irregularly contoured sites Hypoallergenic Multi-Directional Stretch More Information SDS Manufacturer # 1528-4 Brand 3M™ Microfoam™ Manufacturer 3M Country of Origin United States Application Medical Tape Color White Color Range White/Beige/Tan Color Family Dimensions 4 Inch X 5-1/2 Yard HCPCS A4452 Length 4 to 6 Yard Length Material Elastic / Foam Material Range Foam NDC Number 08333152804 Sterility NonSterile UNSPSC Code 42311552 Width 4 Inch Width Latex Free Indicator Not Made with Natural Rubber Latex

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Unique horizontal wicking layer effectively increases capacity by distributing exudate throughout the dressing Soft, nonwoven material helps to provide improved comfort for the patient, along with excellent transpiration Heat-sealed border prevents leakage from the dressing so that the patient remains clean and comfortable for a longer per Adhesive-free Manufacturer # PRD500-100 Brand KerraMax Care® Manufacturer 3M Systagenix/KCI Country of Origin United Kingdom Application Super Absorbent Dressing Border Type Without Border Color White Dimensions 5 X 6 Inch Length 5 to 12 Inch Length Material Nonwoven Shape Rectangle Shape Range Rectangle / Square Sterility Sterile UNSPSC Code 42311545 Width 5 to 6 Inch Width

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The smooth outer film layer helps to reduce shear and friction, create a water- resistant bacterial barrier, and maintain an ideal MVTR A soft inner pouch allows the layers to move freely, absorbing shear and friction forces that can damage peri-wound skin Absorbent core and foam pad combine to lock in exudate , bacteria and MMPs - even under compression A soft silicone layer ensures gentle adhesion, excellent absorption rate and non traumatic removal Horizontal and vertical wicking layer efficiently increases absorption capacity distributing exudate throughout the dressing Manufacturer # CWL1023 Brand KerraFoam™ Gentle Border Manufacturer 3M Systagenix/KCI Country of Origin United Kingdom Adhesive Type Silicone Adhesive Application Foam Dressing Backing Material Film Backing Border Type With Border Color Tan Dimensions 6-7/10 X 6-9/10 Inch Length 5 to 12 Inch Length Material Foam Shape Sacral Shape Range Sacral Sterility Sterile UNSPSC Code 42311546 Width 5 to 6 Inch Width

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The smooth outer film layer helps to reduce shear and friction, create a water- resistant bacterial barrier, and maintain an ideal MVTR A soft inner pouch allows the layers to move freely, absorbing shear and friction forces that can damage peri-wound skin Absorbent core and foam pad combine to lock in exudate , bacteria and MMPs - even under compression A soft silicone layer ensures gentle adhesion, excellent absorption rate and non traumatic removal Horizontal and vertical wicking layer efficiently increases absorption capacity distributing exudate throughout the dressing Manufacturer # CWL1135 Brand KerraFoam™ Gentle Border Manufacturer 3M Systagenix/KCI Country of Origin United Kingdom Adhesive Type Silicone Adhesive Application Foam Dressing Backing Material Film Backing Border Type With Border Color Tan Dimensions 7 X 8 Inch Length 5 to 12 Inch Length Material Foam Pad Size 6 X 7 Inch Pad Product Dating

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