BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    HOT BIOPSY FORCEPS

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

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117406589·

    Flyer

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400105·Flyer models are manual wheelchairs intended to...

    MASKS SURGICAL DENTAL

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

    ACU-BAND ACCUPRESSURE WRIST BAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    BATTERY 14.8V, 6.3 AH LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·January 9, 2013

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·November 22, 2010

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 5, 2025