Other products from "QUIDEL CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 30014613336754 RPS-ID-20-U RPS-ID-20-U InflammaDry GOD ANTIGENS, CF (INCLUDING CF CONTROL), ADENOVIRUS 1-33 1 InflammaDry
2 30014613336747 RPS-ID-20 RPS-ID-20 InflammaDry PFQ,JJX MMP-9 test system,Single (specified) analyte controls (assayed and unassayed) 1 InflammaDry
3 30014613336402 Trichomonas Assay M304.U SolanaTrichomonas Assay OUY Trichomonas vaginalis nucleic acid amplification test system 2 Solana
4 30014613336396 Trichomonas Assay M304.S Solana Trichomonas Assay OUY Trichomonas vaginalis nucleic acid amplification test system 2 Solana
5 30014613336082 Group A Strep Assay M301 Solana GAS Assay PGX Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system 2 Solana
6 30014613335580 C1-Inhibitor A037 MicroVue C1-Inhibitor Plus EIA DBA COMPLEMENT C1 INHIBITOR (INACTIVATOR), ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
7 30014613335573 Bp Plus EIA A027 Kit, Quidel Bb Plus JZH FACTOR B, ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
8 30014613335566 CH50 Eq EIA A018 MicroVue CH50 Eq EIA DAE COMPLEMENT C9, ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
9 30014613335559 CIC-C1q Controls A013 MicroVue CIC-C1q Ctrls DAK COMPLEMENT C1Q, ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
10 30014613335542 CIC-Raji EIA A002 MicroVue CIC-Raji EIA CZY COMPLEMENT C1S, ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
11 30014613335535 CIC-C1q EIA A001 MicroVue CIC-C1q EIA DAK COMPLEMENT C1Q, ANTIGEN, ANTISERUM, CONTROL 2 MicroVue
12 30014613333951 Vitamin D EIA 8046 MicroVue Vitamin D EIA MRG SYSTEM, TEST, VITAMIN D 2 MicroVue
13 30014613333944 PTH EIA 8044 MicroVue PTH EIA CEW RADIOIMMUNOASSAY, PARATHYROID HORMONE 2 MicroVue
14 30014613333937 Calcitonin EIA 8043 MicroVue Calcitonin EIA JKR RADIOIMMUNOASSAY, CALCITONIN 2 MicroVue
15 30014613333920 BAP EIA 8012 MicroVue BAP EIA CIN ELECTROPHORETIC SEPARATION, ALKALINE PHOSPHATASE ISOENZYMES 2 MicroVue
16 30014613333913 PYD EIA 8010 Kit, McVu PYD JMM COLUMN CHROMATOGRAPHY & COLOR DEVELOPMENT, HYDROXYPROLINE 1 MicroVue
17 30014613333906 DPD EIA 8007 Kit, McVu DPD JMM COLUMN CHROMATOGRAPHY & COLOR DEVELOPMENT, HYDROXYPROLINE 1 MicroVue
18 30014613311140 Parainfluenza Virus Assay M114 Lyra Parainfluenza Assay OOU Parainfluenza multiplex nucleic acid assay 2 Lyra
19 30014613311133 Adenovirus Assay M113 Lyra Adenovirus Assay OCC Respiratory virus panel nucleic acid assay system 2 Lyra
20 30014613311126 Direct Strep Assay M112 Lyra Direct Strep Assay PGX Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system 2 Lyra
21 30014613311058 Direct C. difficile Assay M105 Lyra Direct CDIFF Assay OZN,OOI C.Difficile toxin gene amplification assay,real time Nucleic acid amplification system 2 Lyra
22 30014613311027 Direct HSV 1+2/VZV Assay M102 Lyra Direct HSV 1+2/VZV Assay PGI Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutane Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutaneous lesion samples 2 Lyra
23 30014613202783 20278 20278 Solana instrument NSU Instrumentation for clinical multiplex test systems 2 Solana
24 30014613003458 00345 00345 QkVue InLine Strep A Ctrl Set GTY ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP. 1 QuickVue In-Line
25 30014613003434 00343 00343 QkVue InLine Strep A 25T GTZ ANTISERA, ALL GROUPS, STREPTOCOCCUS SPP. 1 QuickVue In-Line
26 30014613336686 RPS-AD RPS-AD AdenoPlus GOD ANTIGENS, CF (INCLUDING CF CONTROL), ADENOVIRUS 1-33 1 AdenoPlus
27 30014613339724 20402 20402 QuickVue At-Home OTC COVID-19 Test QKP Coronavirus antigen detection test system. QuickVue
28 30014613339687 20399 20399 QuickVue At-Home OTC COVID-19 Test QKP Coronavirus antigen detection test system. QuickVue
29 30014613339670 20398 20398 QuickVue At-Home OTC COVID-19 Test QKP Coronavirus antigen detection test system. QuickVue
30 30014613339373 20387 20387 QuickVue® SARS Antigen Test QuickVue
31 30014613331469 20189 20189 QkVue Flu A+B 20K-T, Bulk GNX ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C 1 QuickVue
32 30014613331452 20163 20163 QkVue Strep A Dpstk, 4T Samp GTY ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP. 1 QuickVue
33 30014613320098 0W009 0W009 QkVue H pylori gII 10T LYR Helicobacter pylori 1 QuickVue
34 30014613312123 Group A Strep Assay M212 AmpliVue GAS Assay PGX Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system 2 AmpliVue
35 30014613312116 Trichomonas Assay M211 AmpliVue Trichomonas Assay OUY Trichomonas vaginalis nucleic acid amplification test system 2 AmpliVue
36 30014613312109 HSV 1+2 Assay M210 AmpliVue HSV 1+2 Assay OQO Herpes simplex virus nucleic acid amplification assay 2 AmpliVue
37 30014613312093 Bordetella Assay M209 AmpliVue Bordetella Assay OZZ Bordetella pertussis dna assay system 2 AmpliVue
38 30014613312024 GBS Assay M202 AmpliVue GBS Assay NJR Nucleic acid amplification assay system, group b streptococcus, direct specimen test 1 AmpliVue
39 30014613312017 C. difficile Assay M201 AmpliVue CDiff Assay OZN C.Difficile toxin gene amplification assay 2 AmpliVue
40 30014613202226 20222 20222 QkVue RSV 10, 25T GQG ANTIGEN, CF (INCLUDING CF CONTROLS), RESPIRATORY SYNCYTIAL VIRUS 1 QuickVue
41 30014613202059 iFOB Test 20205 QuickVue iFOB Test Dev Kit 100T KHE REAGENT, OCCULT BLOOD 2 QuickVue
42 30014613202042 iFOB Test 20204 QuickVue iFOB Collect Kit 40T KHE REAGENT, OCCULT BLOOD 2 QuickVue
43 30014613202011 iFOB Test 20201 QuickVue iFOB Tray Pack 50T KHE REAGENT, OCCULT BLOOD 2 QuickVue
44 30014613201977 20197 20197 QkVue iFOB Control Set KHE REAGENT, OCCULT BLOOD 2 QuickVue
45 30014613201960 iFOB Test 20196 QuickVue iFOB Collect Kit 10T KHE REAGENT, OCCULT BLOOD 2 QuickVue
46 30014613201946 iFOB Test 20194 QuickVue iFOB 20T KHE REAGENT, OCCULT BLOOD 2 QuickVue
47 30014613201939 20193 20193 QkVue RSV 20T MCE,GQG RESPIRATORY SYNCYTIAL VIRUS - ELISA,ANTIGEN, CF (INCLUDING CF CONTROLS), RESPIRA RESPIRATORY SYNCYTIAL VIRUS - ELISA,ANTIGEN, CF (INCLUDING CF CONTROLS), RESPIRATORY SYNCYTIAL VIRUS 1 QuickVue
48 30014613201830 20183 20183 QkVue Flu A+B 25T, CE GNX ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C 1 QuickVue
49 30014613201526 20152 20152 QkVue Strep A Dpstk 10T GTY ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP. 1 QuickVue
50 30014613201250 20125 20125 QkVue Strep A Dpstk 25T GTY ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP. 1 QuickVue
Other products with the same Product Code "LYR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 03573026509231 30192-01 VIDAS® H. pylori IgG (HPY) is an automated qualitative test for use on theVIDAS® VIDAS® H. pylori IgG (HPY) is an automated qualitative test for use on theVIDAS® instruments , for the detection of anti-Helicobacter pylori IgG antibodies in human serum or plasma (EDTA). VIDAS® H. pylori IgG BIOMERIEUX SA
2 00893029002571 GIS-62-2ML GIS-62-2ML Urease Glycerol Solution Urease GI SUPPLY, INC.
3 00893029002519 GIS-22 GIS-22 HpFast detects the urease enzyme for the presumptive identification of Helicobac HpFast detects the urease enzyme for the presumptive identification of Helicobacter pylori gastric mucosal biopsies. It is intended for in-vitro diagnostic use only. HpFast GI SUPPLY, INC.
4 00893029002502 GIS-64 GIS-64 HpOne detects the urease enzyme for the presumptive identification of Helicobact HpOne detects the urease enzyme for the presumptive identification of Helicobacter pylori in gastric mucosal biopsies. It is intended for in-vitro diagnostic use only. HpOne GI SUPPLY, INC.
5 00857031002639 T5051B The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative d The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. H. PYLORI CHEK TECHLAB, INC.
6 00857031002622 20343 The QuickVue TLI H. pylori Stool Antigen Test is a rapid membrane enzyme immunoa The QuickVue TLI H. pylori Stool Antigen Test is a rapid membrane enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single use cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. QuickVue TLI H. pylori Stool Antigen Test TECHLAB, INC.
7 00857031002561 20343 The QuickVue TLI H. pylori Test is a rapid membrane enzyme immunoassay for the q The QuickVue TLI H. pylori Test is a rapid membrane enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single use cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. QuickVue TLI H. pylori Test TECHLAB, INC.
8 00857031002523 30996 The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative d The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. H. PYLORI CHEK TECHLAB, INC.
9 00857031002516 30925 The TECHLAB® H. PYLORI QUIK CHEK™ test is a rapid membrane enzyme immunoassay fo The TECHLAB® H. PYLORI QUIK CHEK™ test is a rapid membrane enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single use cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. H. PYLORI QUIK CHEK TECHLAB, INC.
10 00857031002509 T5051 The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative d The TECHLAB® H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. H. PYLORI CHEK TECHLAB, INC.
11 00857031002493 T5050 The TECHLAB® H. PYLORI QUIK CHEK™ test is a rapid membrane enzyme immunoassay fo The TECHLAB® H. PYLORI QUIK CHEK™ test is a rapid membrane enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single use cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. H. PYLORI QUIK CHEK TECHLAB, INC.
12 00855574005414 HP20 H. Pylori, Immunochromatographic Poly stat POLYMEDCO, INC.
13 00850487007654 H. pylori A Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
14 00850487007647 H. pylori A Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
15 00850487007531 H.pylori G 01550Q-1 Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
16 00850487007159 H.pylori G 01550Q-1 Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
17 00840733102271 760130 760130 Curian HpSA, for use with the Curian Analyzer is a rapid, qualitative, fluoresce Curian HpSA, for use with the Curian Analyzer is a rapid, qualitative, fluorescent immunoassay for the detection of Helicobacter pylori antigen in human stool. Test results are intended to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. Accepted medical practice recommends that testing by any current method, to confirm eradication, be done at least four weeks following completion of therapy. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms. Curian HpSA MERIDIAN BIOSCIENCE, INC.
18 00840733101779 710030 710030 The ImmunoCard H. pylori enzyme immunoassay (EIA) is an in vitro qualitative pro The ImmunoCard H. pylori enzyme immunoassay (EIA) is an in vitro qualitative procedure for the detection of IgG to Helicobacter pylori in human serum, plasma, or whole blood. Test results are intended to aid in the diagnosis of H. pylori infection. The ImmunoCard H. pylori assay may be performed in clinical laboratories and physician's offices. ImmunoCard H. pylori MERIDIAN BIOSCIENCE, INC.
19 00840733101731 606096 606096 Premier H. pylori is an enzyme immunoassay (EIA) for the in vitro qualitative de Premier H. pylori is an enzyme immunoassay (EIA) for the in vitro qualitative detection of IgG antibodies to Helicobacter pylori in human serum and plasma. Test results are intended to aid in the diagnosis of H. pylori infection. PREMIER H. pylori MERIDIAN BIOSCIENCE, INC.
20 00840733101670 601396 601396 The Premier Platinum HpSA PLUS enzyme immunoassay (EIA) is an in vitro qualitati The Premier Platinum HpSA PLUS enzyme immunoassay (EIA) is an in vitro qualitative procedure for the detection of Helicobacter pylori antigens in human stool. Test results are intended to aid in the diagnosis of H. pylori infection and to monitor response during and post-therapy in patients. Accepted medical practice recommends that testing by any current method, to confirm eradication, be done at least four weeks following completion of therapy. PREMIER Platinum HpSA PLUS MERIDIAN BIOSCIENCE, INC.
21 00840733101427 610190 610190 Curian is an Immunoassay Analyzer designed to automate incubation, results inter Curian is an Immunoassay Analyzer designed to automate incubation, results interpretation and results reporting of immunoassay diagnostic products. Curian is intended for use with Curian fluorescent immunoassay products. Curian-compatible Meridian Bioscience products are described in individual immunoassay package inserts. Curian Analyzer MERIDIAN BIOSCIENCE, INC.
22 00840733101380 750220 750220 The ImmunoCard STAT! HpSA is a rapid in vitro qualitative procedure for the dete The ImmunoCard STAT! HpSA is a rapid in vitro qualitative procedure for the detection of Helicobacter pylori antigens in human stool. ImmunoCard STAT! HpSA MERIDIAN BIOSCIENCE, INC.
23 00817273020037 300-331A 300-331A CMV IgM Capture Lyoph. Ag. Accessory Kit Diamedix DIAMEDIX CORPORATION
24 00816870022741 1475-300 1475-300A Monobind AccuLite Anti-H. Pylori IgM CLIA Kit - 96 Wells MONOBIND, INC.
25 00816870022734 1575-300 1575-300A Monobind AccuLite Anti-H. Pylori IgG CLIA Kit - 96 Wells MONOBIND, INC.
26 00816870022727 1675-300 1675-300A Monobind AccuLite Anti-H. Pylori IgA CLIA Kit - 96 Wells MONOBIND, INC.
27 00816870021102 1425-300 1425-300A Monobind AccuBind Anti-H. Pylori IgM ELISA Kit - 96 Wells MONOBIND, INC.
28 00816870021096 1525-300 1525-300A Monobind AccuBind Anti-H. Pylori IgG ELISA Kit - 96 Wells MONOBIND, INC.
29 00816870021089 1625-300 1625-300A Monobind AccuBind Anti-H. Pylori IgA ELISA Kit - 96 Wells MONOBIND, INC.
30 00742860100161 175 175 OSOM H Pylori 25 Test Kit SEKISUI DIAGNOSTICS, LLC
31 00722066000304 HPY-13C15 HPY-13C15 Rapid Response H. Pylori Test Cassettes - 15 tests/ kit are for the qualitative Rapid Response H. Pylori Test Cassettes - 15 tests/ kit are for the qualitative detection of antibodies to Helicobacter pylori in whole blood, serum, or plasma. Rapid Response BTNX INC
32 00695684330200 33020 A rapid cassette test for the qualitative detection of Helicobabacter pylori in A rapid cassette test for the qualitative detection of Helicobabacter pylori in serum, plasma, or whole blood. AIMSTEP H. PYLORI GERMAINE LABORATORIES, INC
33 00657498000014 6300-020 6300-020 For the Qualitative Detection of IgG Antibodies to Helicobacter pylori (H. pylor For the Qualitative Detection of IgG Antibodies to Helicobacter pylori (H. pylori) in Whole blood, Serum or Plasma. RELY® H.Pylori STANBIO LABORATORY, L.P.
34 00630414989907 10469596 LHPGCM H.Pylori - IMMULITE - CTL IMMULITE® Systems HPG CONTROL H.pylori IgG SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
35 00630414964164 10381272 LKHPG1 Helicobacter pylori IgG Ab - IMMULITE - RGT - 100 Tests IMMULITE®/IMMULITE® 1000 Systems HPG H.pylori IgG SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
36 00630414961644 10381335 L2KHPG6 Helicobacter pylori IgG Ab - IMMULITE - RGT - 600 Tests IMMULITE® 2000 Systems HPG H.pylori IgG SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
37 00630414961637 10381336 L2KHPG2 Helicobacter pylori IgG Ab - IMMULITE - RGT - 200 Tests IMMULITE® 2000 Systems HPG H.pylori IgG SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
38 00630414960944 10385353 L1KIDW1 Infectious Disease Diluent - IMMULITE - CAL IMMULITE® 1000 System ID2 DIL ID2 Sample Diluent SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
39 00613647000519 4581465021 23900535 SURE-VUE H. PYLORI 30/PK Sure-Vue FISHER SCIENTIFIC COMPANY L.L.C.
40 00612479202719 5007 TEST KIT, H PYLORI (10/KT) McKesson MCKESSON MEDICAL-SURGICAL INC.
41 00612479202702 5008 TEST KIT, H PYLORI (25/KT) McKesson MCKESSON MEDICAL-SURGICAL INC.
42 00350770927459 92745 60480 AVANOS* CLOTEST* Rapid Urease Test AVANOS AVANOS MEDICAL, INC.
43 00350770926636 92663 60407 HALYARD* CLOTEST* Jack Bean Urease Control Tablets AVANOS AVANOS MEDICAL, INC.
44 00083059070040 7004 The GAP-IgG is an ELISA test for the qualitative detection of IgG specific antib The GAP-IgG is an ELISA test for the qualitative detection of IgG specific antibodies to Helicobacter pylori (H. pylori) in human serum. It is a serum test which, when used with other clinical information, can be used as an aid in the diagnosis of infection caused by H. pylori. GAP®-IgG (Gastritis and Peptic Ulcer Test) BIOMERICA, INC.
45 B350GSD0110010 GSD01-1001 Gold Standard Diagnostics H. pylori ELISA IgA Test Kit Gold Standard Diagnostics H. pylori ELISA IgA Test Kit GOLD STANDARD DIAGNOSTICS CORPORATION
46 B350GSD0110000 GSD01-1000 Gold Standard Diagnostics Helicobacter pylori IgG ELISA Test Kit Gold Standard Diagnostics H. pylori ELISA IgG Test Kit GOLD STANDARD DIAGNOSTICS CORPORATION
47 50192253013717 1077-25EIA 1077-25EIA H. pylori Stool Antigen ELISA Kit CARDINAL HEALTH CARDINAL HEALTH 200, LLC
48 50192253012239 B1077-25CH B1077-25CH H. pylori Stool Antigen Rapid Test Kit CARDINAL HEALTH CARDINAL HEALTH 200, LLC
49 30014613320104 0W010 0W010 QkVue H pylori gII 30T QuickVue QUIDEL CORPORATION
50 30014613320098 0W009 0W009 QkVue H pylori gII 10T QuickVue QUIDEL CORPORATION