BEUDAMED
    7 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.

    ACUFIT TOTAL HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERI-CATH(TM)

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    BULLET SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    HL20 BUBBLE SENSOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·July 1, 2014

    X-STREAM

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GCJ·November 29, 2012