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

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    BIODESIGN ENT REPAIR GRAFT

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517574343·CoRoent Ant TLIF Ti, 12x11x36mm 0°

    MEYERHOEFER-CHALAZION CURETTE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013001·MEYERHOEFER-CHALAZION CURETTE

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515016729·Masson N.H., 10 1/2", Stainless

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694045407·PrimaLIF LLIF PEEK Implant, 13mm X 18mm X 60mm,...

    SHEAUMANN PL-980

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

    SCINTILLATING FIBER DOSIMETER (SFD), MODEL MT-SFD-1000

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRIGGER HANDLE F/CABLE CUTTER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXZ·January 7, 2021

    BLADE FOR CABLE CUTTER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXZ·January 7, 2021

    BE-PLS 2050

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 26, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·March 6, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 27, 2014

    HLS SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 18, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code LXH·February 10, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    ACTIVELIFE 1 PC - 1 PC DRAINABLE POUCH W/STOMAHESIVE (SH)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code EZQ·September 19, 2014