Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
Human Papillomavirus nucleic acid amplification test kit (Fluorescent Probe-based real-time PCR assay)
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06970895477574
- Basic UDI-DI Code
- B-06970895477574
- Reference
- S01502T2048
- Device Types
- None provided
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Jiangsu Mole Bioscience Co., LTD.
Additional Description
This kit is intended to qualitatively detect the deoxyribonucleic acid (DNA) of 24 types of human papillomavirus (HPV) in women's cervical shedding cell samples, and identify the HPVs as Group 1 (6, 11, 42, 43, 44 or 81), Group 2 (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 or 68) or Group 3 (26, 53, 66, 73 or 82). For professional in-vitro diagnosti
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105041004 | FULL GENOTYPING HIGH-RISK + LOW-RISK HPV - NA REAGENTS |
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