BEUDAMED
    7 results · 28ms · 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 ×

    TINTELIZE PAI-1 KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377096753·RELINE C Screw, 4.0x38mm Reduction FA

    RHS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPOON-BOBBIN DRAIN TUBE W/ WIRE, OTOLOGY

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 25, 2013

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 17, 2014

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 13, 2011