Septodont

BioRoot Flow is a bioceramic root canal sealer that is easy to use and provides excellent results. It is made of calcium silicate, which is a biocompatible material that is naturally found in the body. BioRoot Flow has a unique flowable consistency that makes it easy to inject into the root canal, and it provides excellent adhesion to dentin and gutta-percha. BioRoot Flow is also radiopaque, which makes it easy to visualize during the root canal procedure. BioRoot Flow has been shown to be effective in preventing bacterial leakage and promoting the healing of the periapical tissues. It is a safe and effective root canal sealer that can be used in a variety of clinical situations. Features & benefits Easy – Ready-to-use syringe provides easy extrusion directly into canals and you maintain your preferred obturation technique Successful – Highly-pure calcium silicate mineral formulation (resin-free) means no shrinkage, limited bacterial growth, and increased biocompatibility and bioactivity which reduce the risk of adverse reactions For Everyone – Designed for cold and warm techniques with excellent flow into accessory canals, tight adhesion to dentin and gutta-percha, and reproducible results in all root canal treatments from simple to complex Presentation Item #01E0510 - 1 x 2g syringe, 1 finger grip, 20 intra-oral tips BioRoot™ Flow is a pure mineral calcium silicate root canal sealer, available in premixed 2g syringe for both cold and warm obturation. Item Description: BioRoot™ Flow, (1) 2g syringe, (1) Finger Grip, (20) Replaceable Tips/box (24 Month Shelf Life) (For Sale in the U.S. Only) Supplier Item Code: 01E0510 NDC Item Code: SEP 01E0510 Unit of Measure: BX WEIGHT (POUNDS): 0.1400

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Indications Local dental anesthesia by infiltration or nerve block in adults and pediatric patients. Features & benefits Formulation without vaso-constrictor for specific clinical situations.  Fast onset: 30 to 120 seconds in the maxilla and 1 to 4 minutes for the mandible.  Duration: will ordinarily provide pulpal anesthesia of about 20 minutes in the maxilla, and about 40 minutes in the mandible.  No-methylparaben formulation to avoid allergic reactions on sensitive patients.  No natural rubber latex components to help reduce allergic responses.  Terminal sterilization of product/cartridges for safe use.  Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.  Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.  Ordering informationItem #01A1003 – Box containing 5 blisters of 10 x 1.7ml glass cartridges  Safety informationReactions to Scandonest® are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Scandonest® is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of mepivacaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. Scandonest® 2% L contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.  

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