BEUDAMED
    6 results · 20ms · 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.

    MICROTEK PISTON & WIRE PROSTHESES

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

    ARGEDENT 45

    FDA 510(k)
    FDA Class 2 ·Dental

    DANEK RING FIXATOR (DRF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN DEPUY ACET. SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code HWC·June 26, 2014

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 3, 2013

    PROMOTE PLUS CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010