Other products from "ARLINGTON SCIENTIFIC, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00816057021192 NC-909001 NC-909001 Detection of Syphilis GMP Antisera, Control For Nontreponemal Tests 2 ASI Disposible Stirrer Pipet
2 00816057021185 NC-5071-002-500 NC-5071-002-500 Disposable Pipet, 500/bag GTO Anti-Streptokinase 1 ASI Disposible Stirrer Pipet
3 00816057021123 NC-987X30LCA NC-987X30LCA Detection of Syphilis, 30 Well, Cutsom GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
4 00816057021116 NC-987X30 NC-987X30 Detection of Syphilis, 30 Well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
5 00816057021109 NC-987X15 NC-987X15 Detection of Syphilis, 15 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
6 00816057021093 NC-987X10E NC-987X10E Detection of Syphilis, 10 well, Export GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
7 00816057021086 NC-987530LCA NC-987530LCA Detection of Syphilis, 30 well, custom GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
8 00816057021079 NC-987530E NC-987530E Detection of Syphilis, 30 well, Export GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
9 00816057021062 NC-987530 NC-987530 Detection of Syphilis, 30 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
10 00816057021055 NC-987515 NC-987515 Detection of Syphilis, 15 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
11 00816057021048 NC-987510LCA NC-987510LCA Detection of Syphilis, no controls, 10 well, custom GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
12 00816057021031 NC-987510 NC-987510 Detection of Syphilis, no controls, 10 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
13 00816057021017 NC-987110LCA NC-987110LCA Detection of Syphilis, no controls, custom GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
14 00816057021000 NC-987110 NC-987110 Detection of Syphilis, no controls ASI RPR Card Test for Syphilis
15 00816057020881 NC-90010000-30 NC-90010000-30 Detection of Syphilis, 30 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
16 00816057020874 NC-90010000-10 NC-90010000-10 Detection of Syphilis, 10 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
17 00816057020867 NC-9005000-30T NC-9005000-30T Detection of Syphilis, 30 Well, TDH GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
18 00816057020850 NC-9005000-30E NC-9005000-30E Detection of Syphilis, Export, 30 Well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
19 00816057020843 NC-9005000-30 NC-9005000-30 Detection of Syphilis, 30 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
20 00816057020836 NC-9005000-10T NC-9005000-10T Detection of Syphilis, 10 well, TDH GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
21 00816057020812 NC-9005000-10 NC-9005000-10 Detection of Syphilis, 10 well GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
22 00816057020805 NC-900500T NC-900500T Detection of Syphilis, TDH GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
23 00816057020799 NC-900500E NC-900500E Detection of Syphilis, Export GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
24 00816057020782 NC-900500-NYE NC-900500-NYE Detection of Syphilis, Export, 3x3ml GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
25 00816057020775 NC-900500-NEO NC-900500-NEO Detection for Syphilis, Export, No Controls GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
26 00816057020768 NC-900500-FD NC-900500-FD Detection of Syphilis, Export (French) GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
27 00816057020751 NC-900500 NC-900500 Syphilis screening test - Nontreponemal GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
28 00816057020744 NC-900100E NC-900100E Detection of Syphilis, Export GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
29 00816057020720 NC-900100-FD NC900100-FD Detection of Syphilis, Export (French) GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
30 00816057020713 NC-900100 NC-900100 Detection of Syphilis GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
31 00816057020706 NC-900025E NC-900025E Syphilis Screening Test, Export GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
32 00816057020690 NC-900025 NC-900025 Syphilis Screening Test GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Card Test for Syphilis
33 00816057020614 NC-860096-AG NC-860096-AG Detection of Mumps antibody LJY Enzyme Linked Immunoabsorbent Assay, Mumps Virus 1 ASI Mumps IgG EIA Test
34 00816057020577 NC-830096-AG NC-830096-AG Detection of Herpes Simplex 1 and 2 Antibodies LGC Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific 2 ASI HSV IgG EIA Test
35 00816057020515 NC-800096-AG NC-800096-AG Detection of Rubella Virus Antiboby LFX Enzyme Linked Immunoabsorbent Assay, Rubella 2 ASI Rubella IgG EIA Test
36 00816057021642 NC-705001 NC705001 Detection of Rheumatoid Factor DHR System, Test, Rheumatoid Factor 2 ASI RF Direct Slide Test Control Set
37 00816057021628 NC-505001 NC-505001 Detection of C-Reactive Protein DCN System, Test, C-Reactive Protein 2 ASI CRP Control Set
38 00816057021253 NC-909002 NC-909002 Detection of Syphilis GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Dispensing Bottle
39 00816057021246 NC-90900210 NC-90900210 Detection of Syphilis GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Dispensing Bottle
40 00816057021239 NC-5072-002 NC-5072-002 Blunt, 20 gauge needle cover GMP Antisera, Control For Nontreponemal Tests 2 ASI RPR Dropper Needle Cover
41 00816057020997 NC-907132 NC-907132 Detection of Syphilis GMP Antisera, Control For Nontreponemal Tests 2 ASI Syphilis Reference Sera
42 00816057020638 NC-870096-AG NC-870096-AG Detection of Epstein Barr Nuclear Antigen LSE Epstein-Barr Virus, Other 1 ASI EBNA IgG EIA Test
43 00816057020539 NC-810096-AG NC-810096-AG Detection of Toxoplasma Antibody LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii 2 ASI Toxoplasma IgG EIA Test
44 00816057020393 NC-5001000 NC-5001000 Detection of C-Reactive Protein DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
45 00816057020386 NC-500100E NC-500100E Detection of C-Reactive Protein, Export DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
46 00816057020379 NC-500100 NC-500100 Detection of C-Reactive Protein DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
47 00816057020362 NC-500050E NC-500050E Detection of C-Reactive Protein, Export DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
48 00816057020355 NC-500050 NC-500050 Detection of C-Reactive Protein DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
49 00816057020348 NC-500025E NC-500025E Detection of C-Reactive Protein, Export DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
50 00816057020331 NC-500025 NC-500025 Detection of C-Reactive Protein DCN System, Test, C-Reactive Protein 2 ASI CRP Slide Test
Other products with the same Product Code "LFX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 05391516747011 2325361 2325361 Captia™ Rubella IgM Trinity Biotech CLARK LABORATORIES, INC.
2 05391516747004 2325301 2325301 Captia™ Rubella IgG Trinity Biotech CLARK LABORATORIES, INC.
3 05391516746878 828102 Wash Buffer Concentrate Type I, 20X Trinity Biotech CLARK LABORATORIES, INC.
4 05391516746786 617134 Serum Diluent Type I Trinity Biotech CLARK LABORATORIES, INC.
5 05391516746748 616134 Serum Diluent Type I Trinity Biotech CLARK LABORATORIES, INC.
6 05391516746533 525700 Substrate Solution (TMB) Trinity Biotech CLARK LABORATORIES, INC.
7 05391516746526 915401 Stop Solution Trinity Biotech CLARK LABORATORIES, INC.
8 05391516746519 827102 Wash Buffer Concentrate Type I, 20X Trinity Biotech CLARK LABORATORIES, INC.
9 05391516743457 2325360 2325360 Captia™ Rubella IgM Trinity Biotech CLARK LABORATORIES, INC.
10 05391516743440 2325350 2325350 Captia™ Rubella IgM Trinity Biotech CLARK LABORATORIES, INC.
11 05391516743433 2325300 2325300 Captia™ Rubella IgG Trinity Biotech CLARK LABORATORIES, INC.
12 04015630940257 07027796190 07027796190 Elecsys Rubella IgM ROCHE DIAGNOSTICS GMBH
13 04015630940240 07027770190 07027770190 Elecsys Rubella IgG ROCHE DIAGNOSTICS GMBH
14 04015630939275 4618831160 4618831160 Elecsys Rubella IgM Immunoassay ROCHE DIAGNOSTICS GMBH
15 04015630939251 4618793160 4618793160 Elecsys Rubella IgG Immunoassay ROCHE DIAGNOSTICS GMBH
16 03573026138585 30226 VIDAS ® RUB IgG (RBG) assay is a quantitative IA intended for use on VIDAS fami VIDAS ® RUB IgG (RBG) assay is a quantitative IA intended for use on VIDAS family instrument in the determination of IgG antibodies to rubella virus in human serum. VIDAS® RUB IgG BIOMERIEUX SA
17 00850487007395 RUB M Q01-110 Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
18 00850487007388 RUB G Q01-100 Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
19 00850487007074 RUB G Q01-100 Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
20 00850487007067 RUB M Q01-110 Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
21 00847865012577 SW4.1_V1 6653860D Manual & CDs, Rubella & CMV IgM IFU, SW4.1_v1, U.S Only BioPlex 2200 BIO-RAD LABORATORIES, INC.
22 00847865011006 SW4.1_V1 6653870D Rubella & CMV IgM Assay Protocol File CD, SW4.1_v1 BioPlex 2200 BIO-RAD LABORATORIES, INC.
23 00847865010696 25174 25174 Rubella IgM EIA Bio-Rad Laboratories, Inc. BIO-RAD LABORATORIES, INC.
24 00847865010689 25173 25173 Rubella IgG EIA Bio-Rad Laboratories, Inc. BIO-RAD LABORATORIES, INC.
25 00847865003186 SW4_ V3 6653870C Rubella & CMV Assay Protocol File CD, SW4_v3 BioPlex 2200 BIO-RAD LABORATORIES, INC.
26 00847865003179 SW4_V3 6653860C Manual & CDs, Rubella & CMV IgM IFU, SW4_v3, US Only BioPlex 2200 BIO-RAD LABORATORIES, INC.
27 00847865001175 6653850 6653850 Rubella & CMV IgM Reagent Pack BioPlex 2200 BIO-RAD LABORATORIES, INC.
28 00817273020211 720-380 "720-380 VZV IgG Test Kit" Diamedix DIAMEDIX CORPORATION
29 00817273020204 720-370 "720-370 Rubella IgM Test Kit" Diamedix DIAMEDIX CORPORATION
30 00817273020198 720-360 "720-360 Rubella IgG Test Kit" Diamedix DIAMEDIX CORPORATION
31 00816057020522 NC-800096-AM NC-800096-AM Detection of Rubella Virus Antibody ASI Rubella IgM EIA Test ARLINGTON SCIENTIFIC, INC.
32 00816057020515 NC-800096-AG NC-800096-AG Detection of Rubella Virus Antiboby ASI Rubella IgG EIA Test ARLINGTON SCIENTIFIC, INC.
33 00811727015181 T8004-96 T8004-96 Pointe Scientific, Inc. Rubella IgM is for the qualitative detection of human Ig Pointe Scientific, Inc. Rubella IgM is for the qualitative detection of human IgM antibodies to rubella virus in human serum by enzyme immunoassay, to aid in the diagnosis of rubella infection. A positive result is presumptive for the detection of anti-rubella IgM antibodies and presumptive for the diagnosis of acute or recent rubella infection. 96 tests Pointe Scientific, Inc. Rubella IgM POINTE SCIENTIFIC, INC.
34 00811727015174 T8003-96 T8003-96 Pointe Scientific, Inc. Rubella IgG is for the qualitative, semi-quantitative an Pointe Scientific, Inc. Rubella IgG is for the qualitative, semi-quantitative and quantitative detection of human IgG antibodies to rubella virus in human serum by enzyme immunoassay, to aid in the assessment of the patient's immunological response to rubella, and as a qualitative screening test to determine the immune status of individuals, including women of childbearing age. These reagents have not received FDA clearance for use in testing blood or plasma donors. 96 tests Pointe Scientific, Inc. Rubella IgG POINTE SCIENTIFIC, INC.
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