BEUDAMED
    8 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.
    Filters FDA Adverse Event ×

    BIOLOX DELTA, CERAMIC FEMORAL HEAD, M,36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·July 3, 2019

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2019

    NEUTRAL LINER 36 MM I.D. SIZE KK FOR USE WITH 56 MM O.D. SIZE KK SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 27, 2019

    CURLIN ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·MOOG MED DEVICES GROUP·Product code FRN·October 31, 2012

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWP·June 10, 2014

    QUADRA ASSURA MP ICD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·June 22, 2015

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 29, 2016

    IMPLANTABLE DRUG INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·November 7, 2024