BEUDAMED
    9 results · 23ms · 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 ×

    KNEE UNK TIBIAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 1, 2026

    PSN FEM CR CMT CCR

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·December 7, 2023

    FORTIVA

    FDA Adverse Event
    Injury ·TUTOGEN MEDICAL, GMBH·Product code FTM·October 20, 2021

    FORTIVA PORCINE DERMIS

    FDA Adverse Event
    Injury ·TUTOGEN MEDICAL GMBH·Product code FTM·April 23, 2021

    BMT 360 TIBIA AUGMENT 71X15MM RL/LM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 13, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·August 14, 2008

    POLY C-LARC-OMCP-VISUB (BH3000)

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZF·May 16, 2011

    NAVIO HANDPIECE

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·August 20, 2020

    FORTIVA

    FDA Adverse Event
    Injury ·TUTOGEN MEDICAL, GMBH·Product code FTM·April 14, 2022