Other products from "SERIM RESEARCH CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M1745100A1 5100A 5100A Serim® GUARDIAN™ RESIDUAL CHLORINE Test Strips indicate the concentration of chl Serim® GUARDIAN™ RESIDUAL CHLORINE Test Strips indicate the concentration of chlorine bleach (sodium hypochlorite) remaining in the solution used to rinse dialysate lines following disinfection of hemodialysis equipment. FKJ Filter, Blood, Dialysis Serim® GUARDIAN™ Residual Chlorine Test Strips
2 M17451671 5167 5167 SERIM GUARDIAN HiSENSE ULTRA 0.1 Test Strips indicates low levels of total chlor SERIM GUARDIAN HiSENSE ULTRA 0.1 Test Strips indicates low levels of total chlorine (chloramines/free chlorine) in feed water used to prepare dialysate. The test also indicates the concentration of residual chlorine (chlorine bleach) remaining in the water used to rinse dialysate lines following disinfection of hemodialysis equipment. MSY Strip, Test, Reagent, Residuals For Dialysate, Disinfectant Serim® GUARDIAN™ HiSENSE ULTRA 0.1™ Test Strips
3 M17451211 5121 5121 Serim® DISINTEK™ OPA Test Strips are chemical indicators for use in determining Serim® DISINTEK™ OPA Test Strips are chemical indicators for use in determining whether the concentration of ortho-phthalaldehyde, the active ingredient in CIDEX® OPA Solution and MetriCide® OPA Plus™ Solution, is above or below the established minimum effective concentration (MEC) of 0.3%. JOJ Indicator, Physical/Chemical Sterilization Process Serim® DISINTEK™ OPA Test Strips
4 M1745119C 5119C 5119C Serim® GUARDIAN™ Blood Leak Test Strips provide a rapid method to test dialysate Serim® GUARDIAN™ Blood Leak Test Strips provide a rapid method to test dialysate for blood if a dialyzer membrane leak is suspected during thehemodialysis procedure. FJD Detector, Leak, Blood Serim® GUARDIAN™ Blood Leak Test Strips
5 M17451121 5112 5112 Serim® GUARDIAN™ Residual Formaldehyde Test Strips measure the concentration of Serim® GUARDIAN™ Residual Formaldehyde Test Strips measure the concentration of formaldehyde remaining after rinsing dialyzers or dialysate lines prior to use in hemodialysis. LIF Dialyzer Reprocessing System Serim® GUARDIAN™ Residual Formaldehyde Test Strips
6 M1745116A1 5116A 5116A Serim® GUARDIAN™ Bicarb pH II Test Strips are designed to test bicarbonate conce Serim® GUARDIAN™ Bicarb pH II Test Strips are designed to test bicarbonate concentrate and/or final dialysate solutions for the appropriate pH where bicarbonate and acid and water are mixed in closed systems. MNV Strip, Dialysate Ph Indicator Serim® GUARDIAN™ Bicarb pH II Test Strips
7 M1745100C1 5100C 5100C Serim® GUARDIAN™ Residual Chlorine Test Strips indicating the concentration of c Serim® GUARDIAN™ Residual Chlorine Test Strips indicating the concentration of chlorine bleach (sodium hypochlorite) remaining in the solution used to rinse dialysate lines following disinfection of hemodialysis equipment. FKJ Filter, Blood, Dialysis Serim® GUARDIAN™ Residual Chlorine Test Strips
8 M17451221 5122 5122 Serim PeriScreen Test Strips indicate the presence of leukocytes (white blood ce Serim PeriScreen Test Strips indicate the presence of leukocytes (white blood cells) in peritoneal dialysate effluent. LJX Test, Urine Leukocyte Serim® PeriScreen™ Test Strips
9 M17451091 5109 5109 The Serim® GUARDIAN™ HiSENSE™ Test Kit indicates low levels of total chlorine (c The Serim® GUARDIAN™ HiSENSE™ Test Kit indicates low levels of total chlorine (chloramine and/or free chlorine) in water used to prepare dialysate. FIP Subsystem, Water Purification Serim® GUARDIAN™ HiSENSE™ Test Kit
10 M17451051 5105 5105 Serim® GUARDIAN™ Residual Peroxide Test Strips measure the concentration of pero Serim® GUARDIAN™ Residual Peroxide Test Strips measure the concentration of peroxide remaining in dialysate lines and dialyzers after disinfection with peracetic acid/peroxide-based disinfectants. LIF Dialyzer Reprocessing System Serim® GUARDIAN™ Residual Peroxide Test Strips
11 M1745140S1 05140S 05140S The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens for the presumptive identification of Helicobacter pylori. LYR Helicobacter Pylori Serim® PyloriTek® Test Kit
12 M17451061 5106 5106 SERIM® GUARDIAN™ Peracetic Acid Test Strips indicate the concentration (potency SERIM® GUARDIAN™ Peracetic Acid Test Strips indicate the concentration (potency) of peracetic acid in dialyzer reprocessing concentrates such as Renalin® Cold Sterilant, PerAldecide™, Puristeril® 340, Peracidin™ and Micro-X®. JOJ Indicator, Physical/Chemical Sterilization Process Serim® GUARDIAN™ Peracetic Acid Test Strips
13 M1745136A1 5136A 5136A Serim DISINTEK GTA 1.5% Test Strips are used to determine whether the glutaralde Serim DISINTEK GTA 1.5% Test Strips are used to determine whether the glutaraldehyde concentration is above or at/below the Minimum Effective Concentration (MEC) of 1.5% for CIDEX® or MetriCide® reusable glutaraldehyde high-level disinfectants. MED Sterilant, Medical Devices Serim® DISINTEK™ GTA 1.5% Test Strips
14 M1745116B1 5116B 5116B Serim® GUARDIAN™ BICARB pH II Test Strips are designed to test bicarbonate conce Serim® GUARDIAN™ BICARB pH II Test Strips are designed to test bicarbonate concentrate and/or final dialysate solutions for the appropriate pH where bicarbonate and acid and water are mixed in closed systems. MNV Strip, Dialysate Ph Indicator Serim® GUARDIAN™
Other products with the same Product Code "LYR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10815845020079 01P53-25 Signify® ALERE SAN DIEGO, INC.
2 10815845020048 92405 Clearview® ALERE SAN DIEGO, INC.
3 10796918001846 05-9494 INSTANT-VIEW H. Pylori Whole Blood/Serum Cassette Test INSTANT-VIEW H. Pylori Whole Blood/Serum Cassette Test ALFA SCIENTIFIC DESIGNS, INC.
4 10796918001839 05-9475 INSTANT-VIEW H. pylori Rapid Test INSTANT-VIEW H. pylori Rapid Test ALFA SCIENTIFIC DESIGNS, INC.
5 10796918001822 05-9473 INSTANT-VIEW H. Pylori Serum Cassette Test INSTANT-VIEW H. Pylori Serum Cassette Test ALFA SCIENTIFIC DESIGNS, INC.
6 10796918001815 05-9472 INSTANT-VIEW H. Pylori Serum Cassette Test INSTANT-VIEW H. Pylori Serum Cassette Test ALFA SCIENTIFIC DESIGNS, INC.
7 10763924392206 ID392 ACCUTEST H. Pylori Rapid Test Device (Whole Blood/Serum) *CLIA-Waived* ACCUTEST H. Pylori Rapid Test Device (Whole Blood/Serum) *CLIA-Waived* JANT PHARMACAL CORPORATION
8 10743816001591 BSP-406WB-25-02 Status™ H. pylori card; 25 Test kit Status™ H. pylori card PRINCETON BIOMEDITECH CORPORATION
9 10743816001584 BSP-406WB-10-02 Status™ H. pylori card; 10 Test kit Status™ H. pylori card PRINCETON BIOMEDITECH CORPORATION
10 10743816001164 BSP-406WB-30-07 BSP-406WB-30-07 Status™ H. pylori card; 30 Test kit- CE (Procedure Card) Status™ H. pylori card PRINCETON BIOMEDITECH CORPORATION
11 10743816001157 BSP-406WB-30-05 BSP-406WB-30-05 BioSign® H. pylori card; 30 Test kit (Procedure Card) BioSign® H. pylori card PRINCETON BIOMEDITECH CORPORATION
12 10743816001140 BSP-406WB-10-01 BSP-406WB-10-01 BioSign® H. pylori card; 10 Test kit; CE BioSign® H. pylori card PRINCETON BIOMEDITECH CORPORATION
13 10743816001133 BSP-406WB-35-01 BSP-406WB-35-01 BioSign® H. pylori card; 35 Test kit; CE BioSign® H. pylori card PRINCETON BIOMEDITECH CORPORATION
14 10722355002023 IHP-30 Qualitative immunoassy of the detection of anti-helicobacter pylori antibodies Detector H. pylori IMMUNOSTICS COMPANY, INC
15 10722355002016 IHP-10 Qualitative immunoassy of the detection of anti-helicobacter pylori antibodies Detector H. pylori IMMUNOSTICS COMPANY, INC
16 10304040155742 5702778 5702778 Henry Schein One Step + H. Pylori Henry Schein HENRY SCHEIN, INC.
17 10304040024154 9004071 9004071 One Step + H Pylori Test Henry Schein HENRY SCHEIN, INC.
18 M220P0800953 P080095 P080095 PRO ADVANTAGE H PYLORI TEST TUBES 20TST/KT PRO ADVANTAGE NATIONAL DISTRIBUTION & CONTRACTING, INC.
19 M1745140S1 05140S 05140S The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens for the presumptive identification of Helicobacter pylori. Serim® PyloriTek® Test Kit SERIM RESEARCH CORPORATION
20 M1745140K1 05140K 05140K The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens The Serim PyloriTek Test Kit detects urease activity in gastric biopsy specimens for the presumptive identification of Helicobacter pylori. Serim® PyloriTek® Test Kit SERIM RESEARCH CORPORATION
21 08426950593805 708720 1. 1x H. pylori IgA ELISA microwell plate, (12-1 x 8 wells), with holder2. 1x 1. 1. 1x H. pylori IgA ELISA microwell plate, (12-1 x 8 wells), with holder2. 1x 1.2mL prediluted ELISA Negative Control 3. 1x 1.2mL prediluted H. pylori IgA ELISA Low Positive4. 1x 1.2mL prediluted H. pylori IgA ELISA High Positive5. 1x 50mL HRP Sample Diluent6. 1x 25mL HRP Wash Concentrate, 40x concentrate7. 1x 10mL HRP IgA Conjugate, (goat), anti-human IgA8. 1x 10mL TMB Chromogen9. 1x 10mL HRP Stop Solution, 0.344M Sulfuric Acid QUANTA Lite® H.pylori IgA ELISA INOVA DIAGNOSTICS, INC.
22 08426950593256 708715 1. 1x H. pylori IgG ELISA microwell plate (12-1 x 8 wells), with holder2. 1x 1.2 1. 1x H. pylori IgG ELISA microwell plate (12-1 x 8 wells), with holder2. 1x 1.2mL prediluted ELISA Negative Control 3. 1x 1.2mL prediluted H. pylori IgG ELISA Low Positive4. 1x 1.2mL prediluted H. pylori IgG ELISA High Positive5. 1x 50mL HRP Sample Diluent6. 1x 25mL HRP Wash Concentrate, 40x concentrate7. 1x 10mL HRP IgG Conjugate, (goat), anti-human IgG8. 1x 10mL TMB Chromogen9. 1x 10mL HRP Stop Solution, 0.344M Sulfuric Acid QUANTA Lite® H.pylori IgG ELISA INOVA DIAGNOSTICS, INC.
23 08305900070040 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.
24 05391516748834 1206651 1206651 Uni-Gold™ H. pylori Antigen Control, 1 Positive and 1 Negative Trinity Biotech MARDX DIAGNOSTICS, INC.
25 05391516748827 1206650 1206650 Uni-Gold™ H. pylori Antigen, 20 Tests Trinity Biotech MARDX DIAGNOSTICS, INC.
26 05391516747738 41-9002 41-9002 Marsorb G, 10.0 mL Trinity Biotech MARDX DIAGNOSTICS, INC.
27 05391516747721 40-1013 40-1013 10x Wash Solution, 100 mL Trinity Biotech MARDX DIAGNOSTICS, INC.
28 05391516747714 40-1006 40-1006 EIA Color Developer, 13.0 mL Trinity Biotech MARDX DIAGNOSTICS, INC.
29 05391516747516 2346401 2346401 Captia H. pylori IgG Trinity Biotech CLARK LABORATORIES, INC.
30 05391516743686 2326430 2326430 Captia™ H. pylori IgA Trinity Biotech CLARK LABORATORIES, INC.
31 05391516743679 2346400 2346400 Captia™ H. pylori IgG Trinity Biotech CLARK LABORATORIES, INC.
32 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
33 00893029002571 GIS-62-2ML GIS-62-2ML Urease Glycerol Solution Urease GI SUPPLY, INC.
34 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.
35 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.
36 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.
37 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.
38 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.
39 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.
40 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.
41 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.
42 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.
43 00855574005414 HP20 H. Pylori, Immunochromatographic Poly stat POLYMEDCO, INC.
44 00850487007654 H. pylori A Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
45 00850487007647 H. pylori A Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
46 00850487007531 H.pylori G 01550Q-1 Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) SeraQuest QUEST INTERNATIONAL, INC.
47 00850487007159 H.pylori G 01550Q-1 Helicobacter pylori immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) ReQuest QUEST INTERNATIONAL, INC.
48 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.
49 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.
50 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.