For in vitro diagnostic use. Others Elecsys Syphilis IVD Elecsys® Syphilis CPS_000515 09015051162 Syphilis Elecsys E2G 20 x 300 Elecsys Syphilis 07613336183083 Reagents, kits 20x300 tests cobas pro serology solution true 09015051190 Syphilis Elecsys E2G 300 V2 Elecsys Syphilis 07613336171998 Reagents, kits 300 tests cobas e 402/801 true 09014977190 Syphilis Elecsys cobas e 100 V2 Elecsys Syphilis 07613336171950 Reagents, kits 100 tests cobas e 411/601/602 true 06923348190 Syphilis Elecsys cobas e 100 Elecsys Syphilis 04015630934881 Reagents, kits 100 tests cobas e 411/601/602 true 09015035190 Syphilis Elecsys cobas e 200 V2 Elecsys Syphilis 07613336171974 Reagents, kits 200 tests cobas e 411/601/602 true 07251378190 Syphilis Elecsys E2G 300 Elecsys Syphilis 04015630940356 Reagents, kits 300 tests cobas e 402/801 true 07802960190 Syphilis Elecsys cobas e 200 Elecsys Syphilis 04015630946501 Reagents, kits 200 tests cobas e 411/601/602 true 09015051502 Elecsys Syphilis en 2 FF000000067E1A0E FF0000000671600E 09015051162 2497 cobas e 801 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useElecsys Syphilis is an in vitro immunoassay for the qualitative detection of total antibodies (IgG and IgM) to Treponema pallidum in human serum and plasma. Elecsys Syphilis is intended to screen individual human donors, including volunteer donors of whole blood and blood components. This test is also intended to be used to screen organ, tissue and cell donors, when donor samples are obtained while the donor’s heart is still beating. It is not intended for use on cord blood specimens. The electrochemiluminescence immunoassay “ECLIA” is intended for use with the cobas pro serology solution equipped with cobas e 801 analytical unit. en 09015051500 Elecsys Syphilis en 1 FF00000004802C0E FF00000004802C0E 09015051190 2497 cobas e 801 9494 cobas e 402 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 09015051501 Elecsys Syphilis en 3 FF00000006E8110E FF000000050B1C0E 09015051190 2497 cobas e 801 9494 cobas e 402 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative detection of total antibodies (IgG and IgM) to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection in conjunction with a nontreponemal laboratory test and clinical signs and symptoms.The Elecsys Syphilis immunoassay is not intended for use in screening blood or tissue donors. The effectiveness of this assay in testing blood or tissue donors has not been established.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 09014977500 Elecsys Syphilis en 1 FF0000000487FC0E FF0000000487FC0E 09014977190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 09014977501 Elecsys Syphilis en 2 FF00000006E8140E FF0000000564660E 09014977190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative detection of total antibodies (IgG and IgM) to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection in conjunction with a nontreponemal laboratory test and clinical signs and symptoms.The Elecsys Syphilis immunoassay is not intended for use in screening blood or tissue donors. The effectiveness of this assay in testing blood or tissue donors has not been established.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 06923348501 Elecsys Syphilis en 3 FF00000003E2280E FF00000001ACE30E 06923348190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative detection of total antibodies (IgG and IgM) to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection in conjunction with clinical signs and symptoms.The Elecsys Syphilis immunoassay is not intended for use in screening blood or tissue donors. The effectiveness of this assay in testing blood or tissue donors has not been established.The electrochemiluminescence immunoassay “ECLIA” is intended for use on Elecsys and cobas e immunoassay analyzers. en 06923348500 Elecsys Syphilis en 7 FF0000000493F90E FF0000000078C10E 06923348190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on Elecsys and cobas e immunoassay analyzers. en 09015035500 Elecsys Syphilis en 1 FF00000004A07E0E FF00000004A07E0E 09015035190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 07251378501 Elecsys Syphilis en 2 FF00000003E2400E FF00000001E2DB0E 07251378190 2497 cobas e 801 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative detection of total antibodies (IgG and IgM) to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection in conjunction with clinical signs and symptoms.The Elecsys Syphilis immunoassay is not intended for use in screening blood or tissue donors. The effectiveness of this assay in testing blood or tissue donors has not been established.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 07251378500 Elecsys Syphilis en 3 FF0000000494360E FF00000001A4100E 07251378190 2497 cobas e 801 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on the cobas e 801 immunoassay analyzer. en 07802960500 Elecsys Syphilis en 4 FF00000004CCA90E FF00000001ECB70E 07802960190 618 cobas e 411 2325 cobas e 602 619 cobas e 601 Product information shown on this page contains elements of the officially released Method Sheet. If you require further information please refer to the full Method Sheet PDF under the given link, or contact your local Roche country representative. Intended useImmunoassay for the in vitro qualitative determination of total antibodies to Treponema pallidum in human serum and plasma. The test is intended as an aid in the diagnosis of syphilis infection.The electrochemiluminescence immunoassay “ECLIA” is intended for use on Elecsys and cobas e immunoassay analyzers. en