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

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    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·May 10, 2021

    GIA 100-3.8 SINGLE USE RELOADABLE

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICAN·Product code GDW·July 30, 2014

    PRECISION SPECTRA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 15, 2019

    DISPOSABLE RADIAL JAW FORCEP

    FDA Adverse Event
    Injury ·SYMBIOSIS·Product code FCL·July 22, 1992

    LIGASURE V SEALER/DIVIDER

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·February 18, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·July 10, 2009

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC·Product code FTL·December 30, 1997

    PROLENE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·May 12, 2026

    PROLENE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·May 12, 2026

    PROLENE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·May 12, 2026

    PROLENE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·May 12, 2026

    THE CLOSER S 6 FR SMC

    FDA Adverse Event
    Death ·PERCLOSE, INC.·Product code MGB·March 5, 2002

    Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZZ·February 20, 2019

    Brand Name: Solana Bordetella Complete Assay Product Name: Solana Bordetella kit Model/Catalog Number: M308 Software Version: not applicable Product Description: One sales unit (kit) contains materials for 48 tests. One kit contains 48 tubes of 1.45 mL Process Buffer and 48 Reaction Tubes. Component: No, not a component

    FDA Recall
    Open, Classified ·Ortho-Clinical Diagnostics, Inc.·Product code OZZ·March 24, 2025

    Bordetella Pertussis Dna Assay System

    FDA classification
    FDA Class 2 ·Bordetella Pertussis Dna Assay System

    OTZ Partners, LLC

    FDA registration
    OTZ Partners, LLC·3 products·🇺🇸 United States

    OMZ-100

    FDA UDI
    GTG Wellness Co., Ltd.·08809520341141·

    OMZ-100

    FDA UDI
    GTG Wellness Co., Ltd.·08809520341134·

    OLZ-200

    FDA UDI
    GTG Wellness Co., Ltd.·08809520341103·

    OMZ-100

    FDA UDI
    GTG Wellness Co., Ltd.·08809520341165·