Semi quantitative test for the detection of Cotinine (Nicotine Metabolite) in a
Semi quantitative test for the detection of Cotinine (Nicotine Metabolite) in a Saliva specimen
Single (Specified) Analyte Controls (Assayed And Unassayed),Glucose Oxidase, Glu
Single (Specified) Analyte Controls (Assayed And Unassayed),Glucose Oxidase, Glucose,System, Test, Blood Glucose, Over The Counter
Semi quantitative test for the detection of Cotinine (Nicotine Metabolite) in a
Semi quantitative test for the detection of Cotinine (Nicotine Metabolite) in a Urine specimen
10-Parameter Urine Reagent Strip For Use with Accustrip URS ReaderBlood, Urobili
10-Parameter Urine Reagent Strip For Use with Accustrip URS ReaderBlood, Urobilinogen, Billirubin, Protein, Nitrite, Ketone, Glucose, pH, SG, Leukocytes
JRE,CDM,JIR,CEN,JMT,JIN,JJB,LJX,JIO,JIL
Refractometer For Clinical Use,Diazonium Colorimetry, Urobilinogen (Urinary, Non
Refractometer For Clinical Use,Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.),Indicator Method, Protein Or Albumin (Urinary, Non-Quant.),Dye-Indicator, Ph (Urinary, Non-Quant.),Diazo (Colorimetric), Nitrite (Urinary, Non-Quant),Nitroprusside, Ketones (Urinary, Non-Quant.),Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.),Test, Urine Leukocyte,Blood, Occult, Colorimetric, In Urine,Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Urine Reagent Strip Reader For Use With Accustrip URS 10 Urine Reagent Strips. *
Urine Reagent Strip Reader For Use With Accustrip URS 10 Urine Reagent Strips. *CLIA-Waived*
ACCUTEST Drug Test Cup 13-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, BUP 10, C
ACCUTEST Drug Test Cup 13-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, BUP 10, COC 300, MDMA 500, MAD 300, MET 1000, OPI 300, OXY 100, PCP 25, TCA 1000, THC 50
ACCUTEST Drug Test Cup 12-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, COC 300,
ACCUTEST Drug Test Cup 12-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, COC 300, MDMA 500, MAD 300, MET 1000, OPI 2000, OXY 100, PCP 25, TCA 1000 ,THC 50
Indicator Method, Protein Or Albumin (Urinary, Non-Quant.),Method, Enzymatic, Gl
Indicator Method, Protein Or Albumin (Urinary, Non-Quant.),Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Drug Test Cup 5 for visual qualitative detection of THC, COC, AMP, BZO, OPI300 (
Drug Test Cup 5 for visual qualitative detection of THC, COC, AMP, BZO, OPI300 (CLIA Waived)
NGL,NFV,NFT,NFY,NFW
Test, Opiates, Over The Counter,Test, Benzodiazepine, Over The Counter,Test, Amp
Test, Opiates, Over The Counter,Test, Benzodiazepine, Over The Counter,Test, Amphetamine, Over The Counter,Test, Cocaine And Cocaine Metabolites, Over The Counter,Test, Cannabinoid, Over The Counter
ACCUTEST - 5 Drug Test Cup *CLIA-Waived*AMP (1000), COC (300), OPI (2000), PCP (
ACCUTEST - 5 Drug Test Cup *CLIA-Waived*AMP (1000), COC (300), OPI (2000), PCP (25), and THC (50)
MultiDrug Test Cup 12+3 AMP,BAR,BUP,BZO,COC,mAMP,MDMA,MOP,MTD,OXY,PCP,THC + Adu
MultiDrug Test Cup 12+3 AMP,BAR,BUP,BZO,COC,mAMP,MDMA,MOP,MTD,OXY,PCP,THC + Adulteration Screen (pH/ S.G./ Oxidant)
ACCUTEST Drug Test Cup 11-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, COC 300,
ACCUTEST Drug Test Cup 11-Panel CLIA-WaivedAMP 1000, BAR 300, BZO 300, COC 300, MAD 300, MET 1000, OPI 2000, OXY, PCP 25, TCA 1000 ,THC 50
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.