Identity
- Trade Name
- HOKAPI™ SAMPLE DILUENT 1 EUDAMED
- Device Name
- HOKAPI™ SAMPLE DILUENT 1 EUDAMED
- Model / Reference
- 010909201 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06971390435052 EUDAMED
- Basic UDI-DI
- 69713904309098Z EUDAMED
- Direct Marketing DI
- 06971390435052 EUDAMED
- EMDN Code
- W0580 IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIES EUDAMED
Classification
- Device Class
- Class A 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
New Device
No
EUDAMED
Hokapi™ Sample Diluent 1 by Suzhou Hokapi Biomedical Engineering Co., Ltd.. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 69713904309098Z | Class A | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Suzhou Hokapi Biomedical Engineering Co., Ltd..
- EUDAMED SRN
- CN-MF-000013723
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 6dfb24ce-6172-4586-b12b-b930ef3f7b52 61 fields · synced Jun 18, 2026