BEUDAMED
    6 results · 21ms · 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 ×

    *

    FDA Adverse Event
    Other ·ZIMMER SPINE, INC.·Product code MCV·August 20, 2004

    SINOVIAL

    FDA Adverse Event
    Injury ·IBSA FARMACEUTICI ITALIA SRL·Product code MOZ·April 20, 2020

    BMT 360 TIBIA AUGMENT 71X15MM LL/RM

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

    SELOX ST 53

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·September 23, 2014

    POLY G (FLOOR)-LARC-OMCP-VISUB-CCD

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

    OPTIPAC 60 REFOBACIN BONE CEMENT R-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·January 28, 2022