BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ALL SILICONE FOLEY CATHETER

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756661102·LAPAROSCOPIC PACK PGYBK

    ULTIMA WHEELCHAIR CUSHION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    MARDX LYME DISEASE IGG IFA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024143791·

    Philips HDI 4000 Ultrasound System Part numbers 9896 053 15031 (8500-0066-01), 9896 053 18811 (8500-0080-01), 9896 053 22011 (8500-0087-01)

    FDA Recall
    Terminated ·Philips Ultrasound, Inc.·Product code DPW·May 6, 2005

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·May 20, 2014

    UNKNOWN RIGHT HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·December 27, 2012

    DURATA STS OPTIM PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 10, 2010