BEUDAMED
    635 results · 57ms · Sources: EU EUDAMED, US FDA

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    GENERAL MEDICAL CO.

    FDA registration
    GENERAL MEDICAL CO.·1 product·🇺🇸 United States

    Changzhou Medical Appliances General Factory Co.,Ltd.

    Manufacturer
    🇨🇳 China

    MEDI-PAK CLEANSING ENEMA SET

    FDA Adverse Event
    Injury ·GENERAL MEDICAL CO.·Product code FCE·April 22, 1994

    NON-ANIMAL CATALASE B-12

    FDA Adverse Event
    Injury ·ALLERGAN PHARMACEUTICALS (IRELAND) LTD INC·Product code LPN·January 30, 1998

    MONOJECT 35 CC SYRINGE

    FDA Adverse Event
    Other ·SHERWOOD DAVIS AND GECK·Product code FMF·November 26, 1997

    MONOJECT 60CC SYRINGE

    FDA Adverse Event
    Other ·SHERWOOD DAVIS AND GECK·Product code FMF·November 26, 1997

    MEDI-PAK LIGHTLY POWDERED EXAM GLOVES

    FDA Adverse Event
    Malfunction ·GENERAL MEDICAL MFG CO.·Product code LYY·October 21, 1996

    BD 10ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMF·July 12, 2004

    CAPIOX SX18 OXYGENATOR

    FDA Adverse Event
    Other ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTZ·April 28, 2005

    FLEXFINDER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·FLEXMEDICS CORP.·Product code FGE·May 13, 1997

    FRESENIUS

    FDA Adverse Event
    Injury ·FRESENIUS USA·Product code KPO·February 4, 1994

    COAGUCHEK XS SYSTEM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code GJS·March 2, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·April 22, 2019

    EUFLEXXA

    FDA Adverse Event
    Injury ·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·October 7, 2022

    NOT SURE OF THE BRAND NAME OF THE CONTACTS

    FDA Adverse Event
    Injury ·*·Product code LPM·November 2, 2004

    DERMAGRAFT-TC

    FDA Adverse Event
    Other ·ADVANCED TISSUE SCIENCES,INC.·Product code MGR·September 14, 1998

    UNK HIP FEMORAL HEAD METAL ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023