BEUDAMED
    46 results · 23ms · Sources: EU EUDAMED, US FDA

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    FIBRI QUIK

    FDA 510(k)
    FDA Class 2 ·Hematology

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668118245·Barraquer NdlHldr, Del, Cvd W/O Lock

    TISSU TRANS FILTRON SYRINGE FILL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    QUADROX-I ADULT WITH AND WITHOUT INTEGRATED ARTERIAL FILTER WITH SOFTLINE COATING, MODEL# HMO 70000, HMO 71000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CUSTOM TUBING - SET INC. OXYGENATOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 24, 2015

    QUADROX COMPLETE PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·November 24, 2014

    HLM TUBING SET W/SOFTLINE COATING

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DWF·July 13, 2015

    QUADROX-I HMO 70000+VHK70000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·July 7, 2015

    SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM

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

    HMO 71000-J#QUADROX-1 ADULT + FILTER

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·March 3, 2015

    HLM TUBING SET W/SOFTLINE COATING

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DWF·July 16, 2015

    HQC 16602-3#HL-SET, OFFENES SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·December 19, 2014

    DESCRIPTION FROM THE CUSTOMER REPORT:

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·August 19, 2016

    QUADROX-I ADULT WITH INTEGRATED FILTER

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·August 17, 2016

    CUSTOM TUBING - SET INCL. HMO 71000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 14, 2015

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 23, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 30, 2013

    CIDEX PLUS 28 DAY SOLUTION

    FDA Adverse Event
    Injury ·ADVANCED STERILIZATION PRODUCTS·Product code LRJ·August 17, 2010

    HLM TUBING SET W/SOFTLINE COATING

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·December 22, 2015

    HLM TUBING SET W/SOFTLINE COATING

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