BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PERMARIDGE HYDROXYLAPATITE MATRIX

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

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E89649603490·Band seating instruments

    PROGUIDE NEEDLE SET

    FDA 510(k)
    FDA Class 2 ·Radiology

    Electronic Sphygmomanometer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FX OXY W/HR & ART FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 23, 2014

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·February 8, 2013

    VIPER TORQUE WRENCH

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC.·Product code HAO·December 16, 2010

    EMBRYO RPLCMNT CATHETER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019