BEUDAMED
    5 results · 20ms · 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.
    Filters FDA Adverse Event ×

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-CLONMEL·Product code MAF·December 17, 2010

    UNKNOWN_KIE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HWC·July 14, 2014

    SYMPHONY OCT SYSTEM AO HANDLE, MEDIUM WITH RATCHET

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code LXH·August 22, 2024