Sentosa SA EBV PCR Test (4X48)
Basic Information
- Primary DI
- 08885013953763
- Basic UDI-DI Code
- B-08885013953763
- Reference
- 300627
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Vela Operations Singapore Pte. Ltd.
Additional Description
The Sentosa® SA EBV Quantitative PCR Test is a real-time PCR-based in vitro diagnostic test intended for use in the detection and quantitation of Epstein-Barr virus (EBV) DNA using Sentosa® SX101 instrument in conjunction with the Rotor-Gene® Q MDx 5plex HRM instrument. For human EDTA plasma, serum and cerebrospinal fluid (CSF) samples, Sentosa® SX Virus Total Nucleic Acid Kit v2.0 (4x24) is used for DNA extraction; and for human EDTA whole blood samples, Sentosa® SX Whole Blood Kit (4x24) is used for DNA extraction. The Sentosa® SA EBV Quantitative PCR Test is intended for use in the detection and quantitation of EBV DNA from symptomatic patients as an aid in EBV diagnosis and the management of transplant or immunocompromised patients who have been diagnosed with EBV infection. The results from the Sentosa® SA EBV Quantitative PCR Test must be interpreted within the context of all relevant clinical and laboratory findings.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105040403 | EBV - NA REAGENTS |
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).