BEUDAMED
    11 results · 25ms · Sources: EU EUDAMED, US FDA

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    SUBMERSIBLE REVERSE OSMOSIS WATER PURIFICATION SYS

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

    InFix®

    FDA UDI
    ZIMMER SPINE, INC.·00889024332034·

    TRABECULAR METAL™

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024306981·

    LONG NAIL KIT R2.0, TI, LEFT GAMMA3 ?11X400MM X 13

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 4, 2012

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 23, 2024

    HYBRITECH DATA STATION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    7200 MICROPROCESSOR VENTILATOR SYSTEM RESPIRATORY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·November 9, 2010

    AQUACEL AG-ANTIMICROBIAL HYDROFIBER DRESSING

    FDA Adverse Event
    Malfunction ·CONVATEC LIMITED·Product code FRO·February 19, 2014

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 16, 2012

    Trabecular Metal acetabular revision system column buttress left posterior/right anterior, 00-4894-300-00, sterile, Zimmer Inc., Parsippany, NJ. Usage: Implantable devices that are used to address bony deficiencies of the pelvic antebulum in revision total hip arthroplasty surgery.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code LPH·April 6, 2010