BEUDAMED
    12 results · 19ms · 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 ×

    DISPOSABLE STEAM BIOLOGICAL TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283846·

    Elastic Lugs

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746133794·LINGUAL ELASTIC LUG FLAT

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209118731·

    Elastic Lugs

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746155055·LINGUAL ELASTIC LUG FLAT

    LED Curing Light

    FDA 510(k)
    FDA Class 2 ·Dental

    FEMSPCE-S DISPOSABLE STERILE VAGINAL SPECULUM, MODEL ST-I

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BOWEL GRASPER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 5, 2014

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code GCX·November 12, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 29, 2010

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·October 14, 2019

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·October 14, 2019