BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    CRX WORLD SHUNT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Rulo Radiofrequency Lesion Probe

    FDA 510(k)
    FDA Class 2 ·Neurology

    POWER STANDING DANI

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SYRINGE PLASTIPAK 1ML INSULIN S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·June 4, 2020

    SYRINGE PLASTIPAK 1ML INSULIN S/SU

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL II LLC - PARSIPPANY, NJ·Product code FMF·February 6, 2025

    SPACEMAKER BLUNT TIP TROCAR 10MM

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code GCJ·February 7, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·August 7, 2014

    Depth Gauge; Catalog Number: 703707; Stryker Trauma AG, CH 2545 Selzach; Distributed in USA by Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. This product is sold separately or as part of Kit # 990256. The depth gauge is an instrument in the VariAx Elbow System. Depth gauges are tools used intra-operatively, to aid in correct screw selection. They can be used with a plate, or directly on bone.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code HTJ·December 22, 2009