BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODIFIED OHMEDA PEEP VALVE (FOR GMS ABSORBER)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517311689·Archon Screw, 4.5x14mm S.T. Variable

    Sterling Supreme Diode Laser

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

    ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 2, 2014

    GYNECARE MORCELLEX TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·October 20, 2010

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 20, 2012

    BD VACUTAINER® VENOUS BLOOD COLLECTION TUBE SERUM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·October 5, 2023