BEUDAMED
    8 results · 18ms · 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.

    DRYALYSATE CONCENTRATE

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

    TEKNAR PROSCAN ACCESSORY PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    HDL CHOLESTEROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014

    400 ML SURGIVAC 1/8 PVC W/ TROCAR

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GCY·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011

    NASAL-AIRE

    FDA Adverse Event
    Malfunction ·INNOMED TECHNOLOGIES·Product code BYE·January 6, 2003

    MENTOR MEMORYGEL BOOST BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·November 13, 2025