BEUDAMED
    34 results · 25ms · 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 Regulation: Us FDA ×

    FORCETRIAD

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

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169413702·BLADE 5102913 29MM WIDE VESSELBLADE 13CM

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964076985·Endo Carry-On Procedure Kit

    Mariner MIS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981293512·Diamond Stylet, Shank

    Arena-L®

    FDA UDI
    SPINEFRONTIER, INC.·00190361038993·Rasp Trial Head, 35X26 Lordotic 12°, 13L

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837026905·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...

    HEADBAND FOR BAHA

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BARD UTAVERSE SMALL VESSEL PTA BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 30, 2025

    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

    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