BEUDAMED
    6 results · 18ms · 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.

    PORT-O-SCOPE(TM)

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

    HANDCARE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TRU-TOUCH VINYL EXAM GLOVES (BELGIUM)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DIGITAL RADIOGRAPHY X-RAY SYSTEM DX-D100

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE N.V.·Product code IZL·June 26, 2014

    ATLAS II HF CRT-D

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

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·November 19, 2012