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Vein Stabilization Device Suppliers

 EMAIL INQUIRY to  4 suppliers  
Donell Inc | Address: The Chrysler Bldg, 405 Lexington Ave, 26th F, New York, New York 10174, USA USA
www.donellskin.com | Send Inquiry | Phone: +1-(800)-3247455
Year Established: 1989  Annual Revenues: < USD 1 Million
Products: Anti-Aging System, Acne Scar Treatments, MCP Anti-Aging System, Anti-Aging clinical System, Skin Nutrition Anti-Aging System, Cosmetic Creams & Lotions, ...
Donell Inc produces specially formulated products for all skin types. Our product line includes lightening cleanser, brightening cream, microdermabrasion and body lotion. Our alpha hydroxy acids gentl more...
 
Clarion Research Group | Address: 35 South Second Ave., Clarion, Pennsylvania 16214, USA USA
Products: Vein Stabilization Device (FDA Code: LBJ), ...
Clarion Research Group specializes in offering medical products. more...
Hartman Enterprises | Address: 5611 Highway 81 North, Williamston, South Carolina 29697, USA USA
Phone: +1-(760)-574-9476
Products: Vein Stabilization Device (FDA Code: LBJ), ...
Hartman Enterprises deals with vein stabilization devices. more...
Halex Istar Ind Farm Ltda. | Address: Br 153, Km 3, Chacara Retiro, Conjunto Caicara, Goiania 74775-027, Brazil
Phone: +62-(3265)-6500
Products: Blood Transfusion Sets (FDA Code: BRZ), Blood & Components Collection Container (FDA Code: KSR), Intravenous Administration Kit (FDA Code: FPA), Vein Stabilization Device (FDA Code: LBJ), ...
Halex Istar Ind Farm Ltda. offers pharmaceutical products. more...
 EMAIL INQUIRY to  4 Vein Stabilization Device suppliers  
FDA Code / Regulation: LBJ / 880.6980

A vein stabilizer is a device consisting of a flat piece of plastic with two noninvasive prongs. The device is placed on the skin so that the prongs are on either side of a vein and hold it stable while a hypodermic needle is inserted into the vein.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 880.9. If the device is not labeled or otherwise represented as sterile, it is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.

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