BEUDAMED
    226 results · 52ms · 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 ×

    PERCLOSE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR DEVICES·Product code MGB·October 31, 2003

    SIGN IM NAIL

    FDA Adverse Event
    Injury ·SIGN FRACTURE CARE INTERNATIONAL·Product code HSB·September 18, 2024

    CADD EXTENSION SETS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·April 13, 2022

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 7, 2017

    SIGN IM NAIL

    FDA Adverse Event
    Injury ·SIGN FRACTURE CARE INTERNATIONAL·Product code HSB·December 13, 2019

    NEURON DELIVERY CATHETER 053

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·April 13, 2009

    4.5MM LCP PROXIMAL TIBIA PL 18 HOLES/334MM RT-STE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code JWH·June 28, 2012

    SCREW

    FDA Adverse Event
    Injury ·Product code HTO·June 28, 2012

    THE SIMPLE LOCKING INTRA-MEDULLARY (SLIM) SYSTEM

    FDA Adverse Event
    Injury ·PEGA MEDICAL INC.·Product code HSB·January 5, 2021

    LOCKING SCREW, FULLY THREADED T2 TIBIA 5X45 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·November 24, 2020

    CROSS PLATE MTP, RIGHT ANCHORAGE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·November 21, 2024

    RIA DRIVESHAFT L520

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HTO·March 6, 2014

    SIGN IM NAIL

    FDA Adverse Event
    Injury ·SIGN FRACTURE CARE INTERNATIONAL·Product code HSB·October 7, 2021

    SCREWDRIVER BLADE, CANNULATED

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code LXH·March 15, 2013

    RADIUS SCREW MULTI-A 4.75 X 35MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-FRANCE·Product code NKB·April 1, 2015

    SAVVY PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·November 20, 2009

    G4 LONG NAIL RIGHT D10XL360MM X 125DEG

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HSB·June 5, 2023

    FEMORAL NAIL GT, RIGHT T2 ALPHA FEMUR ANTEGRADE Ø10X360MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·December 26, 2022

    UNKNOWN -TITANIUM STERNAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·March 10, 2015

    FEMORAL NAIL, COMPRESSION S2 Ø11X400 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 8, 2019