BEUDAMED
    11 results · 28ms · 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 ×

    Tetric PowerFill

    FDA 510(k)
    FDA Class 2 ·Dental

    STRIDE UNICONDYLAR KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR

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

    CER OPTION TYPE 1 TPR SLEVE -3 PE 1

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 22, 2018

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 1, 2024

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014

    SWAN-GANZ THERMODILUTION VENOUS INFUSION PORT (VIP) CATHETER W/AMC THROMBOSHIELD

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DYG·July 28, 2011

    DEPUY ASR XL FEM IMP SIZE 59

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWY·June 21, 2013

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 9, 2023

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JPI·December 17, 2024

    XP-XP Tibial Tray - Interlok 65 mm Item # 195752

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019