BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    FIXATION DEVICE, TRACH TUBE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    WHISK-R

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    JACOB CHUCK

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    MICRO OSCILLATING SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·October 20, 2010

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·AQUATEC OPERATIONS GMBH·Product code IKX·December 20, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026