BEUDAMED
    8 results · 18ms · 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.

    PATIENT EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239345·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 2.5 12....

    TAP Blood Collection Device

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRIATHLON METAL BACKED PATELLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMPELLA CP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·December 31, 2025

    MA204

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·January 17, 2013

    ON-Q PUMP

    FDA Adverse Event
    Death ·I-FLOW CORP.·Product code MEB·January 11, 2011

    WALLFLEX? COLONIC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MQR·July 28, 2014