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Progesterone(P)Detection Kit(CLIA)
EUDAMEDClass IVD General (EU MDR)
Ref 18-02-0154Model 50 Tests/kit
Identity
- Trade Name
- Progesterone(P)Detection Kit(CLIA) EUDAMED
- Device Name
- Progesterone(P)Detection Kit(CLIA) EUDAMED
- Model / Reference
- 50 Tests/kit EUDAMED18-02-0154 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06974674892824 EUDAMED
- Basic UDI-DI
- B-06974674892824 EUDAMED
- EMDN Code
- W0102050106 PROGESTERONE EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Netherlands 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
Progesterone(P)Detection Kit(CLIA) by Shenzhen Zijian 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-06974674892824 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Shenzhen Zijian Biotechnology Co., Ltd
- EUDAMED SRN
- CN-MF-000022829
- Authorised Representative
- Lotus NL B.V. NL-AR-000000121
Sources (1)
- EUDAMED ff8ad251-fde2-4bcf-8088-3530a8c7ec7a 61 fields · synced Oct 6, 2026