BEUDAMED
    12 results · 21ms · 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 ×

    ROSTAM APPLICATOR TAMPON/ROSTAM NON APPLICATOR TAMPON

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NUPRO®

    FDA UDI
    Dentsply Professional·D0039650641·NUPRO FREEDOM SLIM DPA SOFT

    RELAX-O-GUARD

    FDA 510(k)
    FDA Class 1 ·Dental

    DISPOSABLE CAUTERY ABRASIVE PAD

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NexGen® Complete Knee Solution

    FDA UDI
    Zimmer, Inc.·00889024445987·

    T25 STARDRIVE SHAFT F/MATRIX CANNULATED/LONG

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·November 21, 2016

    STRAIGHT TIP T25 DRIVER-LONG

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·October 14, 2016

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    PINNACLE SECTOR II CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MRA·July 29, 2014

    T25 STARDRIVE SHAFT F/MATRIX CANNULATED/LONG

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE: SYNTHES USA PRODUCTS LLC·Product code HXX·September 10, 2018

    GRAFT PUSHER 8MM

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code LXH·November 21, 2016