BEUDAMED
    30 results · 23ms · Sources: EU EUDAMED, US FDA

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    In2Bones Kirschner wire

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bard® Urine Meter with Bag

    FDA UDI
    C. R. Bard, Inc.·00801741033117·Bard® Urine Meter with Bag

    LACTOSORB SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036067465·

    Insertion Tool

    FDA UDI
    Nucletron B.V.·08717213060975·

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364220·Orthopaedic implant inserter/extractor, reusabl...

    LINK Instruments - Trial implants and size gauges

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364138·Knee tibia prosthesis trial, reusable - Endo Mo...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364213·Orthopaedic implant inserter/extractor, reusabl...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364114·Orthopaedic implantation hammering attachment -...

    LINK Instruments - Trial implants and size gauges

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364145·Knee tibia prosthesis trial, reusable - Endo Mo...

    LINK Instruments - Trial implants and size gauges

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575364152·Knee tibia prosthesis trial, reusable - Endo Mo...

    INTELLIVUE GAS MODULES, MODELS G5 M1019A AND G1 M1013A

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOLARC / SOLRX E-SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BARD® URINE METER WITH BAG

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KNX·July 23, 2025

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·November 1, 2024

    BARD® URINE METER WITH BAG

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·December 22, 2023

    BARD® URINE METER WITH BAG

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·December 19, 2023

    DILATION PRODUCTS

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·December 5, 2023

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 8, 2013

    M-SERIES (DC) HEATED HUMIDIFIER

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·June 17, 2011

    PULSE GEN MODEL 102

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·September 5, 2008