BEUDAMED
    671 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 ×

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000019·DNA Specimen Collection, Saliva

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000132·DNA Specimen Collection, Saliva

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000026·DNA Specimen Collection, Saliva (For Over-the-C...

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000262·DNA Specimen Collection, Saliva (For Assisted C...

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000255·DNA Specimen Collection, Saliva

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000248·DNA Specimen Collection, Saliva

    Oragene Dx

    FDA UDI
    DNA Genotek Inc·00627595000224·DNA Specimen Collection, Saliva (For assisted c...

    ORAGENE DX OGD-500.001

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ORAGENE-DX OGD-500; ORAGENE-DX OGD-575; ORAGENE-DX OXD-525; ORAGENE-DX OYD-500

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Phoenix Ultra Chain

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772895056·U CHAIN OPEN GOLD SPOOL 15 FEET

    3005099803-2019-06128

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCL·December 17, 2019

    UNKNOWN CORTRAK NASOGASTRIC TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·March 10, 2025

    WALLFLEX? DUODENAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MUM·October 8, 2025

    SPEEDBAND SUPERVIEW SUPER 7¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FHN·March 22, 2018

    3005099803-2019-06159

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KGE·December 17, 2019

    PONSKY REPL TUBE -20

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.(BASD)·Product code KNT·February 14, 2006

    3005099803-2019-06156

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCL·December 17, 2019

    PONSKY REPL. TUBE-20

    FDA Adverse Event
    Death ·C.R. BARD, INC. (BASD)·Product code KNT·February 14, 2006

    3005099803-2019-06130

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCL·December 17, 2019

    SPEEDBAND SUPERVIEW SUPER 7

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 15, 2025