Identity
- Trade Name
- Neonatal 17-OH-Progesterone FEIA EUDAMED
- Device Name
- Neonatal 17-OH-Progesterone FEIA EUDAMED
- Model / Reference
- 6199871 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06438172205031 EUDAMED
- Basic UDI-DI
- B-06438172205031 EUDAMED
- EMDN Code
- W0102050107 17 OH PROGESTERONE EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Finland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
Yes
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
Neonatal 17-OH-Progesterone FEIA by Labsystems Diagnostics Oy — 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-06438172205031 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Labsystems Diagnostics Oy
- EUDAMED SRN
- FI-MF-000018281
Sources (1)
- EUDAMED ed44f89b-f3b3-45d3-b95d-163086b2e15d 61 fields · synced Jul 19, 2026