BEUDAMED
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    ELDON SCHOOL KIT SKA 2511-30

    FDA UDI
    Eldon Biologicals A/S·05713494000368·For self-testing of ABO and RhD Blood groups. N...

    ELDON HOME KIT HKA 2511-1

    FDA UDI
    Eldon Biologicals A/S·05713494000054·For self-testing of ABO and RhD Blood groups. N...

    SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NON-PRESCRIPTION SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    EliA MPOs Immunoassay

    FDA registration
    PHADIA AB·2 products·🇸🇪 Sweden

    EliA MPOs Immunoassay

    FDA registration
    PHADIA US INC.·2 products·🇺🇸 United States

    FIDIS VASCULITIS

    FDA registration
    THERADIAG·2 products·🇫🇷 France

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193409·Clis Taylor Retr wide blade

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193423·Turner Warwick Ret Mal Blde

    DG Gel 8 Neutral

    FDA UDI
    DIAGNOSTIC GRIFOLS SA·08437014205008·The DG Gel 8 Neutral card is for the detection ...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193430·Farr Style Spring Retractor single prongs L ...

    DG Gel 8 ABO/Rh+Kell

    FDA UDI
    DIAGNOSTIC GRIFOLS SA·08437014205923·The DG Gel 8 ABO/Rh + Kell card is for the dete...

    DG Gel 8 ABO/Rh+Kell

    FDA UDI
    DIAGNOSTIC GRIFOLS SA·08437014205015·The DG Gel 8 ABO/Rh + Kell card is for the dete...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193379·Middle Arm for Modified Kbel Retractor

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193393·INITIAL INCIS RETR SMSHRT BLADE

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193362·Middle Arm for Modified Kbel Retractor

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193386·Middle Arm for Modified Kbel Retractor

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776193416·Assistant ee Soft Tissue blade standard

    Transcatheter Septal Occluder

    FDA Pre-Market Approval
    FDA Class 3 ·GORE CARDIOFORM Septal Occluder (GSO)

    SYRVIATEK CORP.

    FDA registration
    SYRVIATEK CORP.·1 product·🇺🇸 United States