BEUDAMED
    67 results · 53ms · Sources: EU EUDAMED, US FDA

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    RG Medical USA

    FDA registration
    RG Medical USA·25 products·🇺🇸 United States

    GERATHERM MERCURY FREE FEVER THERMOMETER

    FDA Adverse Event
    Malfunction ·GERATHERM MEDICAL AG, GERMANY-EXCLUSIVELY FOR RG MEDICAL DIAGNOSTICS·Product code FQZ·April 17, 2009

    UNK ATTUNE KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JWH·August 27, 2024

    UNK KNEE PATELLA SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·August 27, 2024

    DUROM ACETABULAR COMPONENT 48/42 CODE H

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·March 5, 2020

    FLUTED STEM MOBILE TIBIAL COMPONENT/PRECOAT FOR CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 3, 2018

    ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 3, 2018

    NEXGEN LPS-FLEX GENDER SPECIFIC POROUS FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·December 14, 2016

    NEXGEN FLUTED STEMMED PRECOAT TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·December 14, 2016

    UNKNOWN KNEE CONSTRUCT SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·November 22, 2024

    EVOLIS TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·February 19, 2010

    CYSTOTOME CYSTOENTEROSTOMY NEEDLE KNIFE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code KNS·August 24, 2021

    HYALGAN

    FDA Adverse Event
    Injury ·FIDIA FARMACEUTICI S.P.A.·Product code MOZ·May 13, 2016

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 12, 2011

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 14, 2015

    OT DELICA LANCING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 22, 2015

    RHA 4

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·November 29, 2023

    VIZIGO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·August 27, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE GMBH·Product code NBW·March 1, 2019

    DC BEAD

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LTD·Product code HCG·September 2, 2015