-
,for, Item ID-
- #1254865
- Microgenics #0039
Toxicology Reagent DRI® Benzodiazepine (BZO) CLIA Non-Waived For Clinical Chemistry Analyzers
REAGENT, IMMUNOASSAY DRI BENZODIAZEPINE 100ML D/S
Features
- The DRI® Benzodiazepine Assay is a homogeneous enzyme immunoassay intended for the qualitative and/or semi-quantitative determination of the presence of benzodiazepines and their metabolites in human urine at a cutoff concentration of 200 ng/mL
- The assay is designed for use with a number of clinical chemistry analyzers
- The DRI Benzodiazepine Assay is intended for use on automated clinical analyzers capable of maintaining a constant temperature, pipetting, mixing reagents, measuring enzymatic rates at 340 nm and timing the reaction accurately can be used to perform this immunoassay
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Product Details Email
Product Specifications
| McKesson # | 1254865 |
|---|---|
| Manufacturer # | 0039 |
| Brand | DRI® |
| Manufacturer | Microgenics |
| Country of Origin | Unknown |
| Application | Toxicology Reagent |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Non-Waived |
| CLIA Classified | CLIA Non-Waived |
| Container Type | Bottle |
| For Use With | For Clinical Chemistry Analyzers |
| Form | Ready-to-Use Liquid |
| Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
| Sample Type | Urine Sample |
| Specialty | Toxicology |
| Storage Requirements | Requires Refrigeration |
| Test Category | Drugs of Abuse |
| Test Method | Homogeneous Enzyme Immunoassay (HEIA) |
| Test Name | Benzodiazepine (BZO) |
| Test Type | Single Drug |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116007 |
| Volume | 100 mL |
Features
- The DRI® Benzodiazepine Assay is a homogeneous enzyme immunoassay intended for the qualitative and/or semi-quantitative determination of the presence of benzodiazepines and their metabolites in human urine at a cutoff concentration of 200 ng/mL
- The assay is designed for use with a number of clinical chemistry analyzers
- The DRI Benzodiazepine Assay is intended for use on automated clinical analyzers capable of maintaining a constant temperature, pipetting, mixing reagents, measuring enzymatic rates at 340 nm and timing the reaction accurately can be used to perform this immunoassay
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