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Address: 800 Prime Place, Hauppauge, New York 11788, USA
www.medical-action.com |
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Phone: +1-(631)-231-4600
FDA Registration: 1030451 Year Established: 1977
Products: Analgesics, Antibiotics & Antibacterials, Approved Chemotherapy Containers, Absorbable Hemostats Surgicel, Adhesive Felt, Arm Dressing, ...
Medical Action Industries Inc. develops & distributes a variety of disposable surgical-related products. We manufacture & distribute operating room disposable supplies, containment systems for medical
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Address: PO Box 12600, Research Triangle Park, North Carolina 27709, USA
www.teleflexmedical.com |
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Phone: +1-(919)-544-8000
FDA Registration: 1044475 Annual Revenues: USD 50-100 Million
Employee Count: ~380
Quality: ISO 9001, CE Certified
Products: Absorbable Sutures (FDA Code:
GAK), General Diagnostic Supplies, General Medical Supplies, General Sutures/Needles, Non-Absorbable Sutures (FDA Code:
GAO), Suture Needles, ...
Teleflex Medical, a division of Teleflex Incorporated, is a supplier of medical devices, surgical instruments & disposable medical products. We are a global outsource provider that focuses on medical
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Address: 811 Kirkland Avenue, Suite 100, Kirkland, Washington 98033, USA
www.lucentmedical.com |
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Phone: +1-(425)-822-3310
Year Established: 1994
Annual Revenues: USD 1-5 Million
Quality: ISO 9001 Certified
Products: Magnetic Locator (FDA Code:
FTZ), Endotracheal Tube Locators, Nasogastric Feeding Tube Locators, ...
Lucent Medical Systems, Inc. specializes in medical devices and systems. Our products include Tubesite feeding tube locator, system charging base, nasogastric feeding tube and cadaver study, Zortran d
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FDA Code / Regulation: FTZ / 886.4445 A permanent magnet is a nonelectric device that generates a magnetic field intended to find and remove metallic foreign bodies from eye tissue.
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 886.9. The device 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.