BEUDAMED
    6 results · 22ms · 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 ×

    RH-801/GS MODEL TRANSQ(R)1

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Blood pressure monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOP DISPOSABLE PLASTIC SYRINGES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 29, 2013

    COLLEAGUE COLOR PUMP CE FRENCHVERSION TIPLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 20, 2010

    LOCKING SCREWDRIVER BODY

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS 3003895575·Product code LXH·July 14, 2014