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.

    NIDEK STEREO DISC CAMERA(3-DX)/NIDEK STEREO FUNDUS CAMERA(3-DXF)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SANARUS V2 TREATMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Duette 100% Silicone Dual-Balloon, Temperature-Sensing Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PENTA

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·January 19, 2011

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code NBW·August 1, 2014

    145-DEG PE 42MM HUM LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·November 19, 2024