BEUDAMED
    32 results · 27ms · Sources: EU EUDAMED, US FDA

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    FIXTEMP C&B

    FDA 510(k)
    FDA Class 2 ·Dental

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169373334·BLADE 5102917 29MM WIDE VESSELBLADE 17CM

    Arena-L®

    FDA UDI
    SPINEFRONTIER, INC.·00190361039013·Rasp Trial Head, 35X26 Lordotic 12°, 17L

    FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HLM TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015

    VKMO 70000 #QUADROX-I HMO 70000+VHK71

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015

    BO-HQV #70600ADULT PACK

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015

    VKMO 11000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015

    BO-HQV 70600 ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015

    RESERVOIR VHK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015

    SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·October 23, 2017

    VENOUS HARDSHELL CARDIOTOMY RESERVOIR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·May 9, 2013

    TA 90 - 4.8 SINGLE USE RELOADABLE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·September 19, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 4, 2011