BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Besmed Bacterial Filter and HMEF

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517085082·

    ASAHI RG3 GUIDEWIRE/ASAHI RG3 SOFT GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AEQUALIS SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·October 18, 2024

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·October 18, 2024

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·October 18, 2024

    SOLERA VOYAGER 5.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HXX·February 5, 2026

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 10, 2014

    INSTATRAK 3500

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·August 17, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 22, 2013

    CD HORIZON SOLERA 5.5/6.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXX·December 9, 2024