Identity
- Trade Name
- FOB Rapid Test EUDAMED
- Device Name
- FOB Rapid Test EUDAMED
- Model / Reference
- TFO-N601B-25 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06936983109413 EUDAMED
- Basic UDI-DI
- 6970277510000BXD EUDAMED
- EMDN Code
- W0101060301 GUAIAC-BASED FAECAL OCCULT BLOOD (CC) 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
FOB Rapid Test by Hangzhou AllTest Biotech Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Unknown
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 6970277510000BXD | Class B | Unknown |
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Manufacturer
- Manufacturer
- Hangzhou Alltest Biotech.Co., Ltd.
- EUDAMED SRN
- CN-MF-000010710
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (1)
- EUDAMED 119e51f6-fec0-4784-aac9-93e4739b3b7e 61 fields · synced May 22, 2026