BEUDAMED
    7 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.

    ELVI BICLOT 816

    FDA 510(k)
    FDA Class 2 ·Hematology

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978159232·SET SCREW EXTRACTOR (REVF)

    ANIMEC, MODELS AM-2S-4 AND AM-2S-5

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KLASSIC KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·May 15, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012

    SIMPLEX P-JAPANESE TWIN PACK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·August 16, 2010