BEUDAMED
    1,748 results · 35ms · Sources: EU EUDAMED, US FDA

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    He Gao Plastic Factory

    FDA registration
    He Gao Plastic Factory·2 products·🇨🇳 China

    JIE GAO PLASTIC PRODUCTS CO., LTD.

    FDA registration
    JIE GAO PLASTIC PRODUCTS CO., LTD.·11 products·🇨🇳 China

    JIE GAO MEDICAL PLASTIC PRODUCTS (MALAYSIA) SDN. BHD.

    FDA registration
    JIE GAO MEDICAL PLASTIC PRODUCTS (MALAYSIA) SDN. BHD.·12 products·🇲🇾 Malaysia

    QUAN ZHOU GAO HAO MAO YI YOU XIAN GONG SI

    FDA registration
    QUAN ZHOU GAO HAO MAO YI YOU XIAN GONG SI·2 products·🇨🇳 China

    RESONANCE STENT SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·October 28, 2021

    RESONANCE STENT SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·October 28, 2021

    SPECIMEN GATE SCREENING CENTER

    FDA Adverse Event
    Malfunction ·WALLAC OY, SUBSIDIARY OF PERKINELMER·Product code JQP·September 4, 2015

    EU ENT4.5MMD 28MML WNO DSTL TP

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code NJE·December 15, 2021

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code NJE·July 7, 2023

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code NJE·September 15, 2017

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·March 6, 2015

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·March 6, 2015

    HAMILTON-C1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·October 10, 2024

    PIPELINE

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

    2520274-2013-05898

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDS·September 6, 2013

    2520274-2013-06285

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 6, 2013

    2520274-2013-05899

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 6, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·September 24, 2015

    2520274-2013-05908

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 6, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 24, 2015