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Vaginal Secretion Analyzer
EUDAMEDClass IVD General (EU MDR)
Ref /Model RT-F600,RT-F610,RT-F620,RT-F630
Identity
- Device Name
- Vaginal Secretion Analyzer EUDAMED
- Model / Reference
- RT-F600,RT-F610,RT-F620,RT-F630 EUDAMED/ EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-60101FP EUDAMED
- Basic UDI-DI
- B-60101FP EUDAMED
- EMDN Code
- W0299 IVD INSTRUMENTS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
Yes
EUDAMED
Vaginal Secretion Analyzer by Shenzhen Reetoo Biotechnology Co., Ltd — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
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-60101FP | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Shenzhen Reetoo Biotechnology Co., Ltd
- EUDAMED SRN
- CN-MF-000011699
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 9c7144ad-1aea-4a5c-ba45-1b98ea166042 61 fields · synced Jun 18, 2026