BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYNOVATOR/INCISOR

    FDA UDI
    Smith & Nephew, Inc.·00885554007145·MTO BLADE SYNOVATOR/INCISOR 4.5 ...

    Disposable

    FDA UDI
    Biomet Orthopedics, LLC·00887868510861·

    DISPOSABLE CORING TREPHINE

    FDA UDI
    Biomet Orthopedics, LLC·00880304401808·

    NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO RTA RETINAL THICKNESS ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RSP SHOULDER

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code KWS·June 27, 2014

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·January 8, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWQ·November 16, 2010