-
,for, Item ID-
- #1268796
- Abbott #07P4224
Immunoassay Reagent Alinity i Cytomegalovirus (CMV) IgG CLIA Non-Waived For Alinity i Analyzer 200 Tests
REAGENT, ALINITY I CMV IGG D/S
Features
- The Alinity i CMV IgG assay is a chemiluminescent microparticle immunoassay (CMIA) used for the qualitative detection of IgG antibodies to cytomegalovirus in human serum, serum separator, and plasma tubes (lithium heparin, lithium heparin separator, and tripotassium EDTA) on the Alinity i system
- The Alinity i CMV IgG assay is to be used as an aid in the diagnosis of infection with cytomegalovirus and as an aid in the determination of serological status to cytomegalovirus in individuals including women of child-bearing age
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Product Details Email
Product Specifications
| McKesson # | 1268796 |
|---|---|
| Manufacturer # | 07P4224 |
| Brand | Alinity i |
| Manufacturer | Abbott |
| Country of Origin | Unknown |
| Application | Immunoassay Reagent |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Non-Waived |
| CLIA Classified | CLIA Non-Waived |
| For Use With | For Alinity i Analyzer |
| Number of Tests | 200 Tests |
| Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
| Sample Type | Serum / Plasma Sample |
| Specialty | Immunoassay |
| Storage Requirements | Requires Refrigeration |
| Test Category | ToRCH |
| Test Format | Cartridge |
| Test Method | Chemiluminescent Microparticle Immunoassay (CMIA) |
| Test Name | Cytomegalovirus (CMV) IgG |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116010 |
| Volume | M: 6.6 mL, R1: 6.1 mL, R2: 10.4 mL |
Features
- The Alinity i CMV IgG assay is a chemiluminescent microparticle immunoassay (CMIA) used for the qualitative detection of IgG antibodies to cytomegalovirus in human serum, serum separator, and plasma tubes (lithium heparin, lithium heparin separator, and tripotassium EDTA) on the Alinity i system
- The Alinity i CMV IgG assay is to be used as an aid in the diagnosis of infection with cytomegalovirus and as an aid in the determination of serological status to cytomegalovirus in individuals including women of child-bearing age
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