BEUDAMED
    18 results · 29ms · 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.

    Sienco, Inc.

    Manufacturer
    🇺🇸 United States

    SIENCO, INC.

    FDA registration
    SIENCO, INC.·2 products·🇺🇸 United States

    Sonoclot® SonACT Kit

    FDA UDI
    SIENCO, INC.·B55880004321·The SonACT Kit is an in vitro diagnostic reagen...

    Sonoclot® Reference Plasma Quality Control Kit

    FDA UDI
    SIENCO, INC.·B55890013181·The Reference Plasma Quality Control Kit is for...

    Sonoclot® aiACT Kit

    FDA UDI
    SIENCO, INC.·B55880004411·The aiACT Kit is an in vitro diagnostic test fo...

    Sonoclot® NonActivated Kit

    FDA UDI
    SIENCO, INC.·B55880004261·The Non-Activated Clotting Test Kit contains th...

    Sonoclot® Reference Viscosity Oil Quality Control Kit

    FDA UDI
    SIENCO, INC.·B55890013021·The Reference Viscosity Oil QC test is a simple...

    Sonoclot® gbACT+ Kit

    FDA UDI
    SIENCO, INC.·B55880004121·The gbACT+ Kit is an in vitro diagnostic reagen...

    Sonoclot® aiACT Kit

    FDA UDI
    SIENCO, INC.·B55880004421·The aiACT Kit is an in vitro diagnostic test fo...

    Sonoclot® gbACT+ Kit

    FDA UDI
    SIENCO, INC.·B55880004111·The gbACT+ Kit is an in vitro diagnostic reagen...

    Sonoclot® NonActivated Kit

    FDA UDI
    SIENCO, INC.·B55880004251·The Non-Activated Clotting Test Kit contains th...

    Sonoclot® kACT Kit

    FDA UDI
    SIENCO, INC.·B55880004001·The kACT Kit is an in vitro diagnostic test for...

    Sonoclot® Coagulation & Platelet Function Analyzer

    FDA UDI
    SIENCO, INC.·B558DP29510·The Sonoclot Coagulation & Platelet Function An...

    Sonoclot® kACT Kit

    FDA UDI
    SIENCO, INC.·B55880004011·The kACT Kit is an in vitro diagnostic test for...

    Sonoclot® SonACT Kit

    FDA UDI
    SIENCO, INC.·B55880004311·The SonACT Kit is an in vitro diagnostic reagen...

    QNET B.V.

    Authorized representative
    🇳🇱 Netherlands·33 Manufacturers·364 Devices

    OMNI-ARC STEM

    FDA Adverse Event
    Injury ·OMNILIFE SIENCE INC.·Product code LPH·October 21, 2019

    CMC Medical Devices & Drugs SL

    Authorized representative
    🇪🇸 Spain·698 Manufacturers·11260 Devices