BEUDAMED
    78 results · 43ms · Sources: EU EUDAMED, US FDA

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    VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-SARS-COV-2 IGG REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code QKO·February 11, 2021

    VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LOM·October 11, 2019

    VITROS IMMUNODIAGNOSTIC PRODUCTS HS TROPONIN I (HSTNI) REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code MMI·May 14, 2026

    VITROS IMMUNODIAGNOSTICS PRODUCTS TSH REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JLW·September 18, 2023

    VITROS IMMUNODIAGNOSTICS PRODUCTS TSH REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JLW·September 18, 2023

    VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·December 11, 2017

    VITROS 5600 INTEGRATED SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·July 18, 2013

    ARCHITECT CA 125 II

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LTK·June 4, 2015

    VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I ES REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code MMI·March 8, 2024

    VITROS IMMUNODIAGNOSTIC PRODUCTS TOTAL B HCG II REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DHA·August 24, 2022

    CARDINAL HEALTH RAPID TEST HCG COMBO 30T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·May 6, 2019

    CARDINAL HEALTH RAPID TEST HCG COMBO 30T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·May 6, 2019

    UNK HIP FEMORAL STEM SUMMIT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 13, 2022

    UNK KNEE TIBIAL INSERT SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022

    UNK HIP ACETABULAR CUP ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022

    UNK KNEE TIBIAL TRAY SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    UNK HIP FEMORAL HEAD METAL ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022

    UNK KNEE FEMORAL SIGMA CR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    XPERT MRSA/SA BC

    FDA Adverse Event
    Death ·CEPHEID·Product code NQX·May 4, 2010