BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

    ANATOMIC PEEK PTC CERVICAL FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VENTURI PHACO PACK

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CORNERSTONE-SR TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 11, 2018

    PITUITARY

    FDA Adverse Event
    MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·November 6, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 18, 2013

    TRANSPAC IV MONITORING KIT

    FDA Adverse Event
    Other ·ICU MEDICAL, INC.·Product code FPA·December 22, 2011

    CORNERSTONE-SR TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·September 7, 2017

    CORNERSTONE-SR® TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 6, 2025

    CORNERSTONE-SR® TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 8, 2024