BEUDAMED
    156 results · 46ms · Sources: EU EUDAMED, US FDA

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    LAUNCH DEVELOPMENT

    FDA registration
    LAUNCH DEVELOPMENT·3 products·🇺🇸 United States

    ORskin

    FDA UDI
    LAUNCH DEVELOPMENT CORPORATION·00860012392605·ORskin Blue is intended for incision, excision,...

    CERNER MILLENNIUM RADNET

    FDA Adverse Event
    Malfunction ·CERNER CORP.·Product code LNX·August 30, 2007

    TANDEM MOBI MOBILE APP

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·December 19, 2025

    INGEVITY? MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NVN·July 24, 2018

    OMNISPAN

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MBI·June 14, 2010

    SPACELABS XHIBIT CENTRAL STATION

    FDA Adverse Event
    Malfunction ·SPACELABS HEALTHCARE INC.·Product code MHX·April 17, 2018

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·June 30, 2016

    BROACH CORAIL AMT 8

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code HTQ·October 31, 2019

    CORAIL AMT COLLAR SIZE 8

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code JDI·October 31, 2019

    MICROVENTION

    FDA Adverse Event
    Injury ·MICROVENTION·Product code HCG·February 25, 2002

    OMNISPAN

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MBI·June 14, 2010

    BREVERA BREAST BIOPSY SYSTEM

    FDA Adverse Event
    Injury ·HOLOGIC, INC·Product code KNW·September 8, 2022

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·August 30, 2016

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·August 30, 2016

    ONE TOUCH

    FDA Adverse Event
    Injury ·LIFESCAN J & J·Product code NBW·February 8, 2016

    OMNISPAN

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MBI·June 14, 2010

    DUREPAIR®

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEDICAL, INC.·Product code GXQ·February 8, 2018

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·June 30, 2016

    UNSPECIFIED BD K2EDTA BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·August 11, 2017