Shop 1 X 4 mL, Double Swab Tip, Tarsum™, Finland
- Application
- Test Category
- Test Type
-
For Use With
- For QC of AmnioTest Swabs (11)
- For Assays Detecting HBsAg and Antibodies to HIV-1, HCV, HBc, CMV, HTLV-I (7)
- For use as Quality Control Urine to Monitor Precision of Laboratory Urine Toxicology Testing Procedures for Analytes listed in Package Insert (7)
- For Clinical Specimen (6)
- For Nucleic Acid Tests (6)
- For Quality Control of Clinical Assays and Training of Laboratory Personnel (6)
- For All Major Systems (5)
- For most Major Instrument Systems (5)
- For Assays Detecting Antibodies to HBs and HAV (4)
- For Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel, Qualitative Molecular Assays (4)
- For Clinical Chemistry Analyzers (4)
- For HPLC and Immunoassay Analyzer (4)
- For Monitoring Response of an Intrument to Detect and Flag HL Interference in a Sample (4)
- For Qualitative Molecular Assays (4)
- For Roche/Hitachi and cobas c Analyzers (4)
- For use with the Emit® II Plus Oxycodone Assay (4)
- Abbott Architect®, Abbott AxSYM®, Abbott i-Stat®, Alere Triage®, Beckman Coulter Access®, Beckman Coulter Synchron Dxi® Systems, bioMérieux VIDAS®, Ortho Vitros® Systems, Roche Cobas Integra® Systems, Roche Elecsys® Systems, Roche Modular® Systems, Siemens Advia Centaur® Systems, Siemens Dimension® Series, Siemens Immulite®, Siemens Stratus®, Tosoh AIA® Systems (3)
- For Abbott ci Systems (3)
- For Automated Immunoassay Systems / Vitros (3)
- For Automated Platforms (3)
- For BN II, BN ProSpec Systems (3)
- For BioLis 24i Chemistry Analyzer (3)
- For Coagulation, Chemistry and Immunoassay Analyzer (3)
- For DRI Creatinine-Detect Assay (3)
- For Determination of Presence of S. Aureus DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (3)
- For General Chemistry Analyzer (3)
- For Monitoring Hemoglobin A1c associated with Diabetes (3)
- For Monitoring Preciscion of Popular Immunoassay Assays (3)
- For Monitoring Precision of Ethanol and Ammonia Test Procedures (3)
- For Monitoring Precision of High-Sensitivity or Next Generation Troponin I or Troponin T Assays on Major Analyzer Systems (3)
- For Monitoring Precision of IA and TDM Assays (3)
- For Monitoring Precision of Laboratory Testing Procedures for Immunoassay Assays (3)
- For Monitoring Precision of Serum Protein Assays (3)
- For Monitoring Values on Abbott CELL-DYN® Analyzers With 3-part and 5-part Differential Analyzers (3)
- For Monitoring the Precision of Specialty Immunoassay Testing (3)
- For Quality Control of Clinical Assays and Training of Laboratory Personnel, Clinical Specimen (3)
- For Quality Control of Clinical Assays and Training of Laboratory Personnel, Qualitative Molecular Assays (3)
- For Roche Hitachi 917 series, Beckman AU (400/600/640/680), Beckman Synchron CX, DXC Analyzer (3)
- For Temperature Compensated and Non-compensated Refractometers (3)
- For Verification of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (3)
- For use with Automated Platforms (3)
- For Advia 120 / 2120 / 2120i Hematology Systems (2)
- For Alinity c Systems (2)
- For Assayed Quality Control Materials For High Sensitive C Reactive Protein Analysis (2)
- For Assays Detecting Antibodies to HIV-2 (2)
- For Citrate PT Test Cuvettes (2)
- For Determination of Presence of Group B Streptococci (GBS) DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (2)
- For Determination of Presence of Viral and Bacterial Nucleic Acids, Verification of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (2)
- For Determination of the Presence of BV DNA Markers (2)
- For Ethyl Alcohol Assay (2)
- For Evaluating Performance of Nucleic Acid Tests for Determination of the Presence of C. Trachomatis, N. Gonorrhoeae and T. Vaginalis DNA (2)
- For Evaluating Test Performance of Molecular Assays which detect Mpox Virus Nucleic Acids (2)
- For Molecular Assays (2)
- For Monitoring Assay Performance of Quantitative in vitro Determination of Albumin in Urine on the Yumizen C1200 Analyzer (2)
- For Monitoring Pecision of LZI Oxycodone Enzyme Immunoassay on a number of Automated Clinical Chemistry Analyzers (2)
- For Monitoring Preciscion of Cardiac Assessment Assays (2)
- For Monitoring Preciscion of Serum Protein Assays (2)
- For Monitoring Precision Of Lipid Assays, With Crp Optimized Hs-Crp Assays (2)
- For Monitoring Precision of Analyte Test Procedures Important to Neonatal Testing (2)
- For Monitoring Precision of Immunoassay-based Oncology Testing Procedures (2)
- For Monitoring Precision of Opioid Tests with Drug Levels Confirmed by GC/MS, LC/MS/MS or Other Methods (2)
- For Monitoring Precision of Urine Chemistry Testing Procedures (2)
- For Monitoring the Precision of Laboratory Testing Procedures for CSF Assays (2)
- For use in Quality Control by Monitoring Accuracy and Precision of HORIBA Medical Methods, listed in the annex, on Clinical Chemistry Analyzers (2)
- For use with Real-Time PCR Thermal Cycler (2)
- For 2,000 ng/mL Opiate Cutoff (1)
- For ABO / Rh Test in Tube Method / Immediate Spin Test (1)
- For ACE® Axcel®, Vet Axcel®, ACE®, Alera® ACE® Clinical Chemistry Systems (1)
- For Accutest® ID750 H.Pylori Rapid Urease Test Systems (1)
- For Accutest® Multi-Drug Dipstick (1)
- For Ace Axcel Chemistry Analyzer (1)
- For AimScreen DOA Tests (1)
- For Assays Detecting Antibodies to HBe (1)
- For Assays Detecting Antibodies to HIV-3 (1)
- For Assays Detecting Antibodies to Human Immunodeficiency Virus Type 1 (1)
- For Assays Detecting Antibodies to Treponema Pallidum (1)
- For Assays Detecting HAV IgM, HBc IgM and Anti-HAV (1)
- For Assays Detecting HBsAg and Antibodies to CMV, HBc, HCV, HIV-1/2, HTLV-I/II, HBsAg and Treponema Pallidum (1)
- For Assays Detecting HBsAg and Antibodies to HIV-1, HCV, HBc, CMV, and HTLV-1 (1)
- For Assays Detecting HBsAg and Antibodies to HIV-1, HCV, HBc, CMV, and HTLV-2 (1)
- For Assays Detecting HBsAg and Antibodies to HIV-1, HCV, HBc, CMV, and HTLV-3 (1)
- For Assays Detecting IgG Antibodies to T. Gondii, Rubella, CMV, and HSV Types 1 and 2 (1)
- For Assays Detecting IgM Antibodies to Hepatitis A Virus (1)
- For Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (1)
- For Commercial Dipsticks (1)
- For Commerical Dipsticks (1)
- For Determination of Presence of C. Difficile DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (1)
- For Determination of Presence of C. Trachomatis DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (1)
- For Determination of Presence of N. Gonorrhoeae DNA, Validation of Clinical Assays, Development of Diagnostic Tests and Training of Laboratory Personnel (1)
- For Determination of the Presence of Respiratory Virus Nucleic Acids (1)
- For Dimension Vista® System (1)
- For Elecsys Anti-HBc II Immunoassay on cobas e Immunoassay Analyzers (1)
- For Evaluating Performance of Nucleic Acid Tests for Determination of Presence of Norovirus Nucleic Acid (1)
- For Evaluating the Performance of Nucleic Acid Tests for Determination of the Prescence of SARS-CoV-2 RNA (1)
- For Laboratory Urine Toxicology Testing Procedures (1)
- For Major Automated Chemistry and Immunoassay Instruments (1)
- For Maternal Quadruple Markers (1)
- For Monitoring Assay Precision for Protein and other Critical Analytes in Cerebrospinal Fluid (1)
- For Monitoring Performance of Molecular Assys (1)
- For Monitoring Precision of Cardiac Assessment Test Methods (1)
- For Monitoring Precision of Urine Dipstick Tests (1)
- For Monitoring the Precision of Laboratory Testing Procedures for Bilirubin and Theophyllline Assays (1)
- For Monitoring the Precision of Urine Dipstick Tests (1)
- For Most Analyzer Measuring 3-part WBC Differentials for up to 14 Parameters (1)
- For Nucleic Acid Testing (1)
- For Ortho VITROS® HIV Combo Assay Used to Detect Antibodies to HIV-1 Group O (1)
- For Point of Care Cups and Cards (1)
- For Point of Care Test Cups and Cards (1)
- For Positive Control for Brucella Abortus Antigens (1)
- For Rapid Drug Screen® Drugs of Abuse Tests (1)
- For Roche / Hitachi cobas c Analyzers (1)
- For Roche Hitachi 917 series, Beckman AU (400/600/640/680), Beckman Synchron CX Analyzer (1)
- For Roche Hitachi, Siemens Dimension® and Beckman Synchron CX, LX and DXC Analyzer (1)
- For Sedimat™ 15 Automated ESR Analyzer (1)
- For StaRRsed Analyzer (1)
- For StepPRO™ Grouping Kit (1)
- For ThyroCheck and CLIAwaived Rapid TSH Cassette (1)
- For Urine Chemistry Testing (1)
- For Validating DRI Fentanyl Assay Calibration (1)
- For Validating Performance of Profile-V MedtoxScan Drugs of Abuse Test System (1)
- For Validating Results Obtained usinf Sure-Vue® RPR Test (1)
- For Verifying Performance of Emit® II Plus Oxycodone Assay (1)
- For Vitros 5600 Integrated System (1)
- For Vitros® 5, 1 FS and 4600 Chemistry Systems and Vitros® 5600 Integrated System (1)
- For Wet Mount Microscopy / Acid-Fast Staining (1)
- For Wet Mount Preparations / For use with India Ink COntrol Kit (1)
- For most Analyzer Systems (1)
- For the Qualitative Determination of Total IgG / IgM and IgG Antibodies to SARS-CoV-2 (1)
- For use as Assayed Quality Control Material to Monitor the Precision of the Pointe Oxycodone Reagent Set on a number of Automated Clinical Chemistry Analyzers (1)
- For use as a Positive Qualitative Quality Control Serum to Monitor the Precision of Laboratory Testing Procedures for the Determination of Immunoglobulin G (IgG) Antibodies to SARS-CoV-2 on Abbott i Systems (1)
- For use as a Quality Control Serum to Monitor the Precision of Laboratory Testing Procedures for the Determination of Immunoglobulin G (IgG) Antibodies to SARS-CoV-2 on Abbott i Systems (1)
- For use as an Unassayed Reactive Quality Control with in vitro Assay Procedures for Determination of SARS-CoV-2 Total IgG / IgM and SARS-CoV-2 IgG in Human Serum or Plasma (1)
- For use in LC / MS or GC / MS Applications for Clinical Chemistry, Urine Drug Testing or Forensic Analysis (1)
- For use in Monitoring the Performance of the VITROS ECi / ECiQ / 3600 Immunodiagnostic Systems and the VITROS 5600 / XT 7600 Integrated Systems when used for the Qualitative Detection of Antibodies to Human Immunodeficiency Virus Types 1, and / or 2 (1)
- For use with Abbott and Diasorin Instruments (1)
- For use with Architect and Alinity Systems (1)
- For use with Architect c (1)
- For use with Architect i, Alinity i and Alinity s Systems (1)
- For use with Assays detecting HIV-1 Antigens (1)
- For use with a variety of General Chemistry Analyzers (1)
- For use with all Hand Held Onsite Drug Screening Devices (1)
- For use with most Major Analyzers (1)
- For use with most Major Chemistry and Immunoassay Platforms (1)
- For use with the Emit® II Plus Buprenorphine Assay (1)
- Hemocue B-Hemoglobin Photometer, Hb 201+ Analyzer, B-Glucose Analyzer, Glucose 201 Analyzer (1)
- Intact PTH, Anti-TG, Anti-TPO, Vitamin D, IGF-I, C-Peptide, and Osteocalcin (1)
- Form
- Levels
- Manufacturer Name
- Trade Agreement Act (TAA) Compliant
- Buy American Act (BAA) Compliant
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- #1094474
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- Bio-Rad Laboratories #12005786
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