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Nucleic Acid Detection Kit for Human Papillomavirus 1618 and other 12 High-Risk…
EUDAMEDClass IVD General (EU MDR)
Ref 25Tests/Kit
Identity
- Device Name
- Nucleic Acid Detection Kit for Human Papillomavirus 1618 and other 12 High-Risk Genotyping EUDAMED
- Model / Reference
- 25Tests/Kit EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970664752307 EUDAMED
- Basic UDI-DI
- B-06970664752307 EUDAMED
- EMDN Code
- W0102039099 TUMOUR MARKERS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
Yes
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Category: Preferentially expressed antigen in melanoma (PRAME) IVD, antibody
Nucleic Acid Detection Kit for Human Papillomavirus 1618 and other 12 High-Risk… by Beijing Kewei Clinical Diagnostic Reagent Inc — Class IVD General — IVDD…
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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-06970664752307 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Beijing Kewei Clinical Diagnostic Reagent Inc
- EUDAMED SRN
- CN-MF-000019125
- Authorised Representative
- Lotus NL B.V. NL-AR-000000121
Sources (1)
- EUDAMED 12b83e94-e7a0-4322-a260-cd5cb0f7d2af 61 fields · synced Jun 17, 2026