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Folate test (Up-converting Phosphor Technology)
EUDAMEDClass B (EU MDR)
Ref HGUPT36Model Please see the IFU
Identity
- Trade Name
- Folate test (Up-converting Phosphor Technology) EUDAMED
- Device Name
- Folate test (Up-converting Phosphor Technology) EUDAMED
- Model / Reference
- Please see the IFU EUDAMEDHGUPT36 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06936700410082 EUDAMED
- Basic UDI-DI
- 6970297531060AB EUDAMED
- EMDN Code
- W0102070103 FOLATE EUDAMED
Classification
- Device Class
- Class B EUDAMED
- Market of Registration
- Germany 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
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Folate test (Up-converting Phosphor Technology) by Beijing Hotgen Biotech Co., Ltd. — Class B — 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 | 6970297531060AB | Class B | Active |
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Manufacturer
- Manufacturer
- Beijing Hotgen Biotech Co., Ltd.
- EUDAMED SRN
- CN-MF-000015566
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (1)
- EUDAMED cb5dc7d9-84ed-4203-adfd-6a125869086c 61 fields · synced Jul 16, 2026