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DELFIA Neonatal IRT kit
EUDAMEDFDA 510(k)Class IVD General (EU MDR)
Ref A005-210510(k) K993697
by Wallac Oy
Identity
- Trade Name
- DELFIA Neonatal IRT kit EUDAMED
- Device Name
- DELFIA Neonatal IRT kit EUDAMED
- Model / Reference
- A005-210 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06438147299515 EUDAMED
- Basic UDI-DI
- B-06438147299515 EUDAMED
- EMDN Code
- W0102019007 IMMUNO REACTIVE TRYPSIN 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 IRT kit by Wallac Oy — Class IVD General — FDA_510K, IVDD — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K993697 | Class IVD General | Active |
| EUDAMED | European Union | CE/IVDD | B-06438147299515 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Wallac Oy
- EUDAMED SRN
- FI-MF-000022620
Sources (2)
- EUDAMED 95f43420-4fa8-4511-b994-9df45f9a081f 85 fields · synced Jun 18, 2026
- FDA 510(k) K993697 1 fields · synced May 18, 2026