BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PowerWire Radiofrequency Guidewire Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ellusa Generator, Ellusa Bayonet Tip, Ellusa RF-Cobb Tip, Ellusa SP-Pack and Tips, Ellusa Tip Set

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

    PROCEARA COPINGS AND PONTIC

    FDA 510(k)
    FDA Class 2 ·Dental

    REPROCESSED DECANAV EP CATHETER, F CURVE

    FDA Adverse Event
    Injury ·STERILMED, INC.·Product code NLH·September 4, 2025

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    MX-PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·July 19, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2013

    LOGIC CR TIB INSERT STD, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 29, 2024

    TRANSMITTER MMT-7841ZN GST5G US

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PQF·August 11, 2025