BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    H-H NERVE ROOT RETRACTOR

    FDA 510(k)
    FDA Class 1 ·Neurology

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR28220481·Betaflex wires Titanium Straight-Arch-F. max. ....

    KETAC-CEM IN REF. TO K802048

    FDA 510(k)
    FDA Class 2 ·Dental

    COLLAGEN TENDON SHEET-D

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INTERPORE CROSS INTERNATIONAL (ICI) OCCIPITO-CERVICO-THORACIC (OCT) ROD AND PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 20, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·October 9, 2012

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code MTA·August 24, 2010