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 ×

    ACS TOTAL IGE IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    DR GREENBURGS HYBRID VACUUM

    FDA 510(k)
    FDA Class 2 ·Dental

    Heel Stick Safety Lancet (HHZ-II, HHZ-III)

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

    ARTHROSCOPE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC.·Product code HRX·December 10, 2010

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 17, 2013

    UNKNOWN DEPUY PINNACLE METAL LINER

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. 8010379·Product code KWY·July 8, 2014