ZIKA VIRUS - NA REAGENTS
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 06928103007112
- Basic UDI-DI Code
- B-06928103007112
- Reference
- DA0711
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Daan Gene Co., Ltd.
Additional Description
The product is intended for qualitative detection of the specific fragment of NS1 gene of Asian and African lineage Zika viruses in serum, plasma, saliva, and urine specimens from individuals with an epidemiological history and symptoms including fever, rash, arthralgia, or conjunctivitis that are difficult to explain by other reasons. During clinical use, relevant laboratory testing requirements shall be complied. The test results of this kit are for clinical reference only, and cannot be used as the sole basis for confirming or excluding cases, and cannot be used for normal population screening.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105040531 | ZIKA VIRUS - NA REAGENTS |
Available In Countries
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).