BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IO FIX, IO FIX PLUS, CARPALFIX, EXTREMITY MEDICAL SCREW AND WASHER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    METAL TRANSCEND ARTICULATION SYSTEM (LARGER SIZES)

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    ELECSYS SHBG CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·June 15, 2023

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LZO·August 12, 2024

    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-1PC DRAINABLE POUCH W/ STOMAHESIVE (SH)

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

    ASR XLA M/L SLEEVE 12/14 +2

    FDA Adverse Event
    Injury ·DEPUY INTL LTD.·Product code KWA·June 1, 2011

    XIA TITANIUM 4.5 BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·September 3, 2020

    SERVO-I BASE UNIT

    FDA Adverse Event
    Injury ·MAQUET CRITICAL CARE AB·Product code CBK·December 5, 2023

    SERVO-I BASE UNIT

    FDA Adverse Event
    Injury ·MAQUET CRITICAL CARE AB·Product code CBK·December 4, 2023