BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    ASTROGLIDE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ASTROGLIDE

    FDA Adverse Event
    Malfunction ·COMBE INC·Product code KMJ·January 16, 2024

    ROMFLEX REHABILITATION EQUIPMENT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    COGAN CORP KITS OF DENTAL HAND INSTRUMENTS

    FDA 510(k)
    FDA Class 1 ·Dental

    HOPKINS TELESCOPE 0°, 5 MM, 29 CM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·May 16, 2025

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013

    GYRUS SINUS THRUCUT

    FDA Adverse Event
    Malfunction ·GYRUS ACMI·Product code LRC·November 29, 2010

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 15, 2014