BEUDAMED
    3,596 results · 19ms · Sources: EU EUDAMED, US FDA

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    4FUSION

    FDA UDI
    Stryker GmbH·07613252263173·4-Fusion Fixation Device

    4FUSION

    FDA UDI
    Stryker GmbH·07613252263159·4-Fusion Fixation Device

    4FUSION

    FDA UDI
    Stryker GmbH·07613252263180·4-Fusion Fixation Device

    ANALYZER: NOVA STAT PROFILE 1 QUA CON MAT: ELECT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Xandrine ren/qua/bei/bast Na/Var-F/Mi-L/Nu S

    Device
    EU MDR · Eu Md Class 1 ·Thanner GmbH·On the market

    DESARA ONE

    FDA Adverse Event
    Injury ·CALDERA MEDICAL·Product code PAH·March 6, 2023

    ALINITY I ANTI-HBC II REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LOM·April 22, 2026

    ALINITY I ANTI-HBC II REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LOM·March 6, 2026

    HEMOPOD

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL SYSTEMS, INC·Product code MHX·September 11, 2024

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·February 24, 2012

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 13, 2025

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·January 8, 2020

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 26, 2020

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 3, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 5, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 2, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 26, 2019

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·February 16, 2012

    12/14 ARTICUL 40MM M SPEC-2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·May 12, 2014