BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    CHARLOTTE (TM) MTP BONE FUSION PLATE SYSTEM HEX SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515019195·Adson Hemo Fcps, cvd, original, 7 1/4"

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037428·Unitek(TM) Bicuspid Band General Purpose Wide L...

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857581128·Split Tube Retractor Ø14x90 mm

    BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200

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

    DIMENSION NT-PROBNP FLEX REAGENT CARTRIDGE METHOD, DIMENSION PBNP CALIBRATOR, MODELS RF423, RC423

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX #3/13 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 27, 2019

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SARL·Product code NJE·December 17, 2021

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 3/13 MM RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 18, 2017

    FEMORAL COMPONENT SPHERE CEMENTED SIZE 3+ R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 7, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2014

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·November 2, 2018

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·April 2, 2019