BEUDAMED
    5,169 results · 21ms · Sources: EU EUDAMED, US FDA

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    LETTINO GEA

    Device
    EU MDR · Eu Md Class 1 ·FISIOTECH srl·On the market

    GEA ELISA Microplate Reader

    Device
    EU IVDR · Eu Ivd Class A ·Linear Chemicals S.L.U·On the market

    ELI 150c

    FDA UDI
    MORTARA INSTRUMENT, INC.·00817655022994·Electrocardiograph

    ELI 150c

    FDA UDI
    MORTARA INSTRUMENT, INC.·00812345025774·Electrocardiograph

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094354966·ELI150c 12-Lead Multi-Channel Electrocardiograp...

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 6, 2007

    AXIOS STENT AND ELECTROCAUTERY ENHANCED DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PCU·May 11, 2023

    ABSOLOK EXTRA ABSORBABLE LIGATING CLIPS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code FZP·March 20, 1998

    MR HISPEED SYSTEM

    FDA Adverse Event
    Other ·GENERAL ELECTRIC MEDICAL SYSTEMS·Product code LNH·April 16, 1998

    GORE PROPATEN VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·March 16, 2009

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·June 30, 2015

    GEA

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·FISIOTECH srl·1 device

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·February 20, 2002

    GE LIGHTSPEED 16 SLICE

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAK·March 5, 2009

    OEC, 9900

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAA·December 26, 2006

    GEA - Microplate Reader

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Linear Chemicals S.L.U·1 device

    SERIES 50 XM FETAL/MATERNAL MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code HGM·September 21, 2011

    LOGIQ E9

    FDA Adverse Event
    Malfunction ·SEE H10·Product code IYN·April 4, 2018

    COMPAX 40E

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS, LLC·Product code IZZ·March 19, 2009

    AXIOS STENT AND ELECTROCAUTERY ENHANCED DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PCU·June 14, 2024