BEUDAMED
    10 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.

    HERPES HOMINUS I-COMPLE FIX ANTIGEN & NEGATIVE CLT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209112784·KIT, TACTICAL OPERATOR RESONSE - BLK - CUSTOM

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

    Ambu SPUR II Adult Resuscitator, Ambu SPUR II Pediatric Resuscitator, Ambu SPUR II Infant Resuscitator

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO VERTE-STACK SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Death ·THORATEC CORP.·Product code DSQ·May 23, 2014

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·November 30, 2012

    DEPUY PINNACLE SECTOR II CUP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY·Product code KWA·September 28, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 8, 2021

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 8, 2021