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HIV 1/2/O Tri-line Human Immunodeficiency Virus Rapid Test Device (Whole Blood …
EUDAMEDClass IVD Annex II List A (EU MDR)
Ref IHI-T402
Identity
- Device Name
- HIV 1/2/O Tri-line Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) EUDAMED
- Model / Reference
- IHI-T402 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06952999407497 EUDAMED
- Basic UDI-DI
- B-06952999407497 EUDAMED
- EMDN Code
- W0105090302 HIV 1 / 2 - RT & POC EUDAMED
- Models / Variants
- Whole Blood EUDAMEDSerum EUDAMEDPlasma EUDAMED
Classification
- Device Class
- Class IVD Annex II List A EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
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
HIV 1/2/O Tri-line Human Immunodeficiency Virus Rapid Test Device (Whole Blood … by Abon Biopharm(Hangzhou) Co., Ltd — Class IVD Annex II List A — IVDD…
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-06952999407497 | Class IVD Annex II List A | Active |
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Manufacturer
- Manufacturer
- Abon Biopharm(Hangzhou) Co., Ltd
- EUDAMED SRN
- CN-MF-000009171
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (1)
- EUDAMED 1abf908d-460f-47ee-96f2-f67f00849a4d 61 fields · synced Jun 18, 2026