BEUDAMED
    7 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 FDA Adverse Event ×

    CER OPT TYPE 1 TPR SLEVE 0MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·June 13, 2019

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 7, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 4, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 21, 2014

    G7 OSSEOTI 3 HOLE SHELL 52MM E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 13, 2019

    ACT ARTIC E1 HIP BRG 28X42MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 13, 2019

    G7 DUAL MOBILITY LINER 42MM E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 13, 2019