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Helicobacter Pylori

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Description
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H. PYLORI QUIK CHEK
TECHLAB, INC.
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.
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H. PYLORI CHEK
TECHLAB, INC.
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.
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H. PYLORI QUIK CHEK
TECHLAB, INC.
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.
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Poly stat
POLYMEDCO, INC.
H. Pylori, Immunochromatographic
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SeraQuest
QUEST INTERNATIONAL, INC.
Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA)
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ReQuest
QUEST INTERNATIONAL, INC.
Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA)
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SeraQuest
QUEST INTERNATIONAL, INC.
Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
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ReQuest
QUEST INTERNATIONAL, INC.
Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
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REMEL
REMEL, INC.
Selective Rapid Urea (0.5ml) 24/PK
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Curian HpSA
MERIDIAN BIOSCIENCE, INC.
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.
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ImmunoCard H. pylori
MERIDIAN BIOSCIENCE, INC.
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.
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PREMIER H. pylori
MERIDIAN BIOSCIENCE, INC.
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.
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PREMIER Platinum HpSA PLUS
MERIDIAN BIOSCIENCE, INC.
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.
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Curian Analyzer
MERIDIAN BIOSCIENCE, INC.
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.
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ImmunoCard STAT! HpSA
MERIDIAN BIOSCIENCE, INC.
The ImmunoCard STAT! HpSA is a rapid in vitro qualitative procedure for the detection of Helicobacter pylori antigens in human stool.
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Diamedix
DIAMEDIX CORPORATION
300-331A CMV IgM Capture Lyoph. Ag. Accessory Kit
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Monobind AccuLite Anti-H. Pylori IgM CLIA Kit - 96 Wells
MONOBIND, INC.
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Anti-H. Pylori IgG AccuLite CLIA Test System - 96 Wells
MONOBIND, INC.
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Anti-H. Pylori IgA AccuLite CLIA Test System - 96 Wells
MONOBIND, INC.
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Anti-H. Pylori IgM AccuBind ELISA Test System - 96 Wells
MONOBIND, INC.
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Anti-H. Pylori IgG AccuBind ELISA Test System - 96 Wells
MONOBIND, INC.
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Anti-H. Pylori IgA AccuBind ELISA Test System - 96 Wells
MONOBIND, INC.
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OSOM H Pylori 25 Test Kit
SEKISUI DIAGNOSTICS, LLC
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Rapid Response
BTNX Inc
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.
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AIMSTEP H. PYLORI
GERMAINE LABORATORIES, INC
A rapid cassette test for the qualitative detection of Helicobabacter pylori in serum, plasma, or whole blood.
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RELY® H.Pylori
STANBIO LABORATORY, L.P.
For the Qualitative Detection of IgG Antibodies to Helicobacter pylori (H. pylori) in Whole blood, Serum or Plasma.
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IMMULITE® Systems HPG CONTROL H.pylori IgG
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
H.Pylori - IMMULITE - CTL
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IMMULITE®/IMMULITE® 1000 Systems HPG H.pylori IgG
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Helicobacter pylori IgG Ab - IMMULITE - RGT - 100 Tests
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IMMULITE® 2000 Systems HPG H.pylori IgG
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Helicobacter pylori IgG Ab - IMMULITE - RGT - 600 Tests
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IMMULITE® 2000 Systems HPG H.pylori IgG
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Helicobacter pylori IgG Ab - IMMULITE - RGT - 200 Tests
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IMMULITE® 1000 System ID2 DIL ID2 Sample Diluent
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Infectious Disease Diluent - IMMULITE - CAL
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Sure-Vue
FISHER SCIENTIFIC COMPANY L.L.C.
SURE-VUE H. PYLORI 30/PK
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McKesson
MCKESSON MEDICAL-SURGICAL INC.
TEST KIT, H PYLORI (10/KT)
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McKesson
MCKESSON MEDICAL-SURGICAL INC.
TEST KIT, H PYLORI (25/KT)
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AVANOS
Avanos Medical, Inc.
AVANOS* CLOTEST* Rapid Urease Test
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AVANOS
Avanos Medical, Inc.
HALYARD* CLOTEST* Jack Bean Urease Control Tablets
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GAP®-IgG (Gastritis and Peptic Ulcer Test)
BIOMERICA, INC.
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.
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MEDLINE
MEDLINE INDUSTRIES, INC.
TEST,H.PYLORI,CASS,25 TEST
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Teco Diagnostics H. pylori Card Test
TECO DIAGNOSTICS
Teco Diagnostics H. pylori Card Test is an immunochromatographic assay for the qualitative determination of IgG antibodies specific to Helicobacter pylori (H. pylori) in human serum. The test is intended for professional use as an aid in the diagnosis of H. pylori infections.
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H. Pylori IgG ELISA
DRG Instruments Gesellschaft mit beschränkter Haftung
The DRG Helicobacter pylori IgG ELISA is an enzyme-linked immunosorbent assay for the qualitative detection of IgG antibodies to H. pylori in sera from symptomatic adults.
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AccuDiag ™
Diagnostic Automation, Inc.
AccuDiag ™ H. pylori Antigen ELISAIntended to be used for the qualitative and/or quantitative detection of antigens from Helicobacter pylori bacteria in a clinical specimen, using an enzyme immunoassay (EIA) method.
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Premier HpSA Flex
MERIDIAN BIOSCIENCE, INC.
The Premier HpSA Flex enzyme immunoassay (EIA) is an in vitro qualitative procedure for the detection of Helicobacter pylori antigens in human stool. The test is intended for use with unpreserved stool specimens or preserved stool specimens in transport media. 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.
0
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H. Pylori IgG ELISA
DRG International Inc
The DRG Helicobacter pylori IgG ELISA is an enzyme-linked immunosorbent assay for the qualitative detection of IgG antibodies to H. pylori in sera from symptomatic adults.
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MedMira Rapid H. Pylori Antibody Test
MedMira Laboratories Inc
The MedMira Rapid H. Pylori Antibody Test is a rapid flow through test developed and manufactured by MedMira Laboratories Inc.
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McKesson
MCKESSON MEDICAL-SURGICAL INC.
TEST KIT, H PYLORI (25/KT)
0
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McKesson
MCKESSON MEDICAL-SURGICAL INC.
TEST KIT, H PYLORI (10/KT)
0
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Hp Detect Stool Antigen ELISA
BIOMERICA, INC.
The Hp Detect™ Stool Antigen ELISA is an in vitro diagnostic qualitative enzyme immunoassay for the detection of Helicobacter pylori (H. pylori) antigens in human stool or feces. The Hp Detect™ Stool Antigen ELISA is intended to aid in the initial diagnosis and post-therapy diagnosis of H. pylori infection. Additionally, the test may be used to assess H. pylori infection status after treatment. Retesting at a minimum of 4 weeks after the completion of treatment may be done to assess H. pylori status. Test results should always be taken into consideration by the physician in conjunction with patient’s clinical information (history and symptoms). For Prescription Use Only.