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I.V. Fluid Transfer Unit Suppliers

 EMAIL INQUIRY to  61 to 62 of 62 suppliers  Page: << Previous 20 Results 1 2 3 [4]
Duoject Medical Systems, Inc. | Address: 50 Chemin De Gaspe, Complex B-5, Bromont, Quebec J2L 2N8, Canada Canada
www.duoject.com | Send Inquiry | Phone: +1-(450)-534-3666/877-534-3666
FDA Registration: 9613744
Products: I.V. Fluid Transfer Unit (FDA Code: LHI), ...
Duoject Medical Systems, Inc. specializes in offering syringes. Our E-Z-Link™ is a vial socket connector with a captured needle. This connector can be packaged separately or in a kit with a drug more...
 
Flextronics International Gmbh | Address: Friesacher Strasse 3, Althofen A-9330, Austria
Phone: +43-(978)-2355643
FDA Registration: 3006126537
Products: Cryosurgical Unit (FDA Code: GEH), Blood Collection Lancet (FDA Code: FMK), Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX), Glucose Oxidase, Glucose (FDA Code: CGA), Glucose Glucose Dehydrogenase (FDA Code: LFR), Diagnostic Ultrasonic Transducer (FDA Code: ITX), ...
Flextronics International Gmbh focuses on blood lancets. more...
 EMAIL INQUIRY to  61 to 62 of 62 I.V. Fluid Transfer Unit suppliers  Page: << Previous 20 Results 1 2 3 [4]
FDA Code / Regulation: LHI / 880.5440

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

Classification. Class II (special controls). The special control for pharmacy compounding systems within this classification is the FDA guidance document entitled "Class II Special Controls Guidance Document: Pharmacy Compounding Systems; Final Guidance for Industry and FDA Reviewers." Pharmacy compounding systems classified within the intravascular administration set are exempt from the premarket notification procedures in subpart E of this part and subject to the limitations in 880.9.

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