BEUDAMED
    6 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.
    Filters Regulation: Us FDA ×

    BENZODIAZEPINE SERUM TOX EIA TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SOMNOSCREEN

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 20, 2014

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 14, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 13, 2011