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Retrograde Flow Check Valve Suppliers

  2 suppliers  
Intl. Medical Industries | Address: 2881 West Mcnab Rd., Pompano Beach, Florida 33069, USA USA
Phone: +1-(954)-917-9570
FDA Registration: 1217831
Products: Filtered IV Admin Sets, Piston Syringe (FDA Code: FMF), Disposable Aspiration and Injection Needle (FDA Code: GAA), Intravenous Administration Kit (FDA Code: FPA), I.V. Fluid Transfer Unit (FDA Code: LHI), Whole Body Nuclear Scanner (FDA Code: JAM), ...
Intl. Medical Industries offers products such as venting needles, tamper evident caps for oral syringes and IV final filters. more...
 
Spirax Sarco, Inc. | Address: 1150 Northpoint Blvd., Blythewood, South Carolina, USA USA
Phone: +1-(800)-575-0394
Year Established: 1983  Annual Revenues: USD 50-100 Million  Employee Count: ~330  Quality: ISO 9001 Certified
Products: Heat and Moisture Exchanger, Retrograde Flow Check Valve (FDA Code: MJF), Steam Filter, ...
Spirax Sarco, Inc. is a supplier of steam system solutions. We supply DIVA flow meter, EasiHeat™ compact heat exchange solution, FTS14 ball float steam trap, BT6 balanced pressure steam trap, an more...
  2 Retrograde Flow Check Valve suppliers  
FDA Code / Regulation: MJF / 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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