BEUDAMED
    515 results · 29ms · Sources: EU EUDAMED, US FDA

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    Amvex Vacuum Regulator

    FDA UDI
    OHIO MEDICAL, LLC·00628101501815·VR-LI series, VacReg, Int 3Mode 200mmHg, Ohio A...

    CHENG LIH INDUSTRIAL CO., LTD.

    FDA registration
    CHENG LIH INDUSTRIAL CO., LTD.·4 products·🇻🇳 Vietnam

    JAAN LIH OPTICAL CO., LTD.

    FDA registration
    JAAN LIH OPTICAL CO., LTD.·1 product·🇹🇼 Taiwan

    JIANN LIH OPTICAL CO., LTD.

    FDA registration
    JIANN LIH OPTICAL CO., LTD.·4 products·🇹🇼 Taiwan

    LIH

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER BIOMEDICAL LTD·Product code JJY·April 5, 2011

    JIANN LIH SAFETY PRODUCTS (M) SDN BHD

    FDA registration
    JIANN LIH SAFETY PRODUCTS (M) SDN BHD·2 products·🇲🇾 Malaysia

    OLYMPUS AUTOMATED CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD.·Product code JJE·October 1, 2002

    OLYMPUS AUTOMATED CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD.·Product code JJE·October 1, 2002

    OLYMPUS AUTOMATED CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD.·Product code JJE·October 1, 2002

    OLYMPUS AUTOMATED CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD.·Product code JJE·October 1, 2002

    FENESTRATED BIPOLAR FORCEPS

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·January 10, 2018

    DXC 700 AU CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC·Product code JJE·November 13, 2025

    BD VACUTAINER® SST¿ II ADVANCE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 19, 2025

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 11, 2011

    PIPELINE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·February 11, 2022

    AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code JGJ·December 8, 2021

    AU5400 CLINICAL CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·October 21, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 8, 2017

    HUT EXT DR FINAL ASSY-STANDARD

    FDA Adverse Event
    Malfunction ·LIEBEL FLARSHEIM·Product code IXR·April 6, 2015

    WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·April 17, 2024