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.

    SONY COLOR VIDEO CAMERAS AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    APTIMA HIV-1 QUANT DX ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code MZF·October 25, 2024

    COMFEEL POWDER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TOP SINGLE USE U.T.W. A-V FISTULA NEEDLE Y TYPE

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

    FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·January 22, 2024

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·June 19, 2014

    VANGUARD DCM CR TIBIAL BEARING 10MM X 71/75MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 27, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 22, 2012