BEUDAMED
    8 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    Everyway Analog OTC TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113554·IMPLANT BLADE 5.2MM (BX/5)

    AMIGO REMOTE CATHETER SYSTEM & ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL OBC-63 BREAST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 14, 2025

    ENDURON 10D 50OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code HRY·November 5, 2008

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 13, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 12, 2013