QuickVue Chlamydia test
QuickVue® Chlamydia offers high sensitivity and specificity -- in all patient populations.
QuickVue® Chlamydia is easy to perform and interpret. A simple extraction procedure requires the addition of only two reagents. Either endocervical swab or cytology brush specimens can be used. The 25 test kit is stored at room temperature.
Features & Benefits
| Feature |
Benefit |
| Rapid Test Results: |
Provides timely results to aid patient management. |
92% Sensitivity (overall)
99% Specificity (overall) |
Accurate, reliable results for cost-effective patient care. |
93.6% Sensitivity (asymptomatic)
99.1% Specificity (asymptomatic): |
Highly accurate in asymptomatic patient population. |
| Two Reagents: |
Easy to perform -- requires minimal training. |
| Two-Color Endpoint: |
Easy to read and interpret results. |
| Self-Contained Test Cassette: |
Clean, easy to use, easy to dispose. Less hands-on time. |
| All Components Included in Kit: |
No need for additional equipment. |
| Room Temperature Storage: |
No refrigerator space needed. No need for reagents to warm up. Tests can be run when needed.
9 months* |
| Technical Support: |
Professional staff available for assistance. |
| * From date of manufacture |
Product Specification
| Method: |
Lateral Flow |
| Time to Result: |
12 minutes, or less |
| Specimen Type: |
Endocervical Swab/Cytology Brush |
| Storage: |
9 months at room temperature* |
| Internal Procedure Controls: |
Yes, positive and negative |
| External Controls: |
Yes, positive and negative included in kit |
| Sensitivity: |
92% (overall) |
| Specificity: |
99% (overall) |
| Catalog Number: |
QUI0B006 |
| Kit Size: |
25 tests per kit |
-FDA 510K, CLIA Classified as Moderately Complex
-Reimbursement Codes: 87810, Amount: $17.52
-It is the individual provider's responsibility to determine appropriate coding, charges and claims for a particular service. Policies regarding appropriate coding and payment levels can vary greatly from payer to payer and change over time. We strongly recommends that providers contact their contracted payers to determine appropriate coding and charge or payment levels prior to submitting claims.
-This test is or medical professional use only and is not intended for personal use.