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Nucleic Acid Detection Kit for High-risk Human Papillomavirus (PCR-Fluorescence…
EUDAMEDClass IVD General (EU MDR)
Ref HPV001
Identity
- Trade Name
- Nucleic Acid Detection Kit for High-risk Human Papillomavirus (PCR-Fluorescence Probing) EUDAMED
- Device Name
- Nucleic Acid Detection Kit for High-risk Human Papillomavirus (PCR-Fluorescence Probing) EUDAMED
- Model / Reference
- HPV001 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06974081870309 EUDAMED
- Basic UDI-DI
- B-06974081870309 EUDAMED
- EMDN Code
- W0105041003 PARTIAL GENOTYPING HIGH-RISK HPV - NA REAGENTS EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Nucleic Acid Detection Kit for High-risk Human Papillomavirus (PCR-Fluorescence… by Singuway Biotech Inc. — Class IVD General — IVDD — listed in EUDAMED
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-06974081870309 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Singuway Biotech Inc.
- EUDAMED SRN
- CN-MF-000027180
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (1)
- EUDAMED 468b5ed6-6898-425a-8abf-00f0ed7aa4f1 61 fields · synced Jun 18, 2026