BEUDAMED
    6 results · 26ms · 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.

    FOLEY CATHETER TUBE HOLDER NO. 101

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CORDIS BIPAL BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DYNATECH MR4000 MICROPLATE READER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 9

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 22, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 7, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014