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

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    QUANTUM CEMENT RESTRICTOR

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257128831·15-20 MV FOR MEN CLSC EW STD GREY VI

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257127735·15-20 MV FOR MEN SEL EW CLF STD GREY VI

    8 GAUGE MICROMARK II TISSUE MARKER, MODELS C1540 & C1535

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

    MPT 24 AND VITAL VIEW 24

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OCTRODE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 3, 2013

    STELLARIS OPTIMIZED STABILITY VACUUM PACK

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQC·February 15, 2011

    ACCURUS 200

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 8, 2008

    Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use

    FDA Enforcement
    Class II ·Terminated·Cadence Science, Inc.·November 20, 2019