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DELFIA Neonatal 17α-OH-progesterone kit
EUDAMEDClass IVD General (EU MDR)
Ref A024-103
by Wallac Oy
Identity
- Trade Name
- DELFIA Neonatal 17α-OH-progesterone kit EUDAMED
- Device Name
- DELFIA Neonatal 17α-OH-progesterone kit EUDAMED
- Model / Reference
- A024-103 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06438147413164 EUDAMED
- Basic UDI-DI
- B-06438147413164 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
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
DELFIA Neonatal 17α-OH-progesterone kit by Wallac 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-06438147413164 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Wallac Oy
- EUDAMED SRN
- FI-MF-000022620
Sources (1)
- EUDAMED 36512dbf-2549-47f6-8ff4-3934a9735d74 61 fields · synced Jun 19, 2026