For in vitro diagnostic use. Others Elecsys Rubella IgM IVD Elecsys® Rubella IgM CPS_000509 04618831160 Rubella IgM Elecsys cobas e 100 Elecsys Rubella IgM 04015630939275 Reagents, kits 100 tests cobas e 411/601/602 true 07027796190 Rubella IgM Elecsys E2G 300 Elecsys Rubella IgM 04015630940257 Reagents, kits 300 tests cobas e 402/801 true 04618831190 Rubella IgM Elecsys cobas e 100 Elecsys Rubella IgM 04015630921461 Reagents, kits 100 tests cobas e 411/601/602 true 09755837190 Rubella IgM Elecsys E2G 100 V1 Rubella IgM Elecsys E2G 100 V1 07613336218440 Reagents, kits 100 tests Not Available true 04618831501 Elecsys Rubella IgM en 10 FF0000000742700E FF000000000F660E 04618831160 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 useThis assay is for the in vitro qualitative determination of IgM antibodies to rubella virus in human serum and heparin, EDTA and citrate plasma. This assay may be used as an aid in the presumptive diagnosis of an acute or recent rubella infection in individuals, including women of childbearing age.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers.NOTE: This assay has not been cleared/approved by the FDA for blood/plasma donor screening. en 07027796501 Elecsys Rubella IgM en 5 FF0000000709EF0E FF00000001DD8B0E 07027796190 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 useThis assay is for the in vitro qualitative determination of IgM antibodies to rubella virus in human serum and heparin, EDTA and citrate plasma. This assay may be used as an aid in the presumptive diagnosis of an acute or recent rubella infection in individuals, including women of childbearing age.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers.NOTE: This assay has not been cleared/approved by the FDA for blood/plasma donor screening. en 07027796500 Elecsys Rubella IgM en 6 FF00000006934A0E FF00000001A4C80E 07027796190 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 IgM antibodies to Rubella virus in human serum and plasma.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 07027796500 Elecsys Rubella IgM en 7 FF00000006DCBC0E FF000000044FCA0E 07027796190 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 IgM antibodies to Rubella virus in human serum and plasma.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en 04618831500 Elecsys Rubella IgM en 14 FF00000005C7390E FF0000000012060E 04618831190 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 IgM antibodies to Rubella virus in human serum and plasma.The electrochemiluminescence immunoassay “ECLIA” is intended for use on Elecsys and cobas e immunoassay analyzers. en 09755837501 Elecsys Rubella IgM en 1 FF0000000730C40E FF0000000722520E 09755837190 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 useThis assay is for the in vitro qualitative determination of IgM antibodies to rubella virus in human serum and heparin, EDTA and citrate plasma. This assay may be used as an aid in the presumptive diagnosis of an acute or recent rubella infection in individuals, including women of childbearing age.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers.NOTE: This assay has not been cleared/approved by the FDA for blood/plasma donor screening. en 09755837500 Elecsys Rubella IgM en 1 FF00000006DCBB0E FF000000065C380E 09755837190 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 IgM antibodies to Rubella virus in human serum and plasma.The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers. en