BEUDAMED
    7 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 ×

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 29, 2022

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 9, 2014

    KUGEL PATCH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 12, 2012

    COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·August 26, 2010

    HYBRID GLENOID GLENOID BASE ARCOM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 29, 2022

    POROUS TITANIUM GLENOID POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 29, 2022

    COMPREHENSIVE SHOULDER SYSTEM MODULAR HEAD VARIABLE OFFEST

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBF·August 29, 2022