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Apteekki Hoitava Nenäsumute Dekspantenoli 25 ml
EUDAMEDClass I (EU MDR)
Ref 9289816
Identity
- Trade Name
- Apteekki Hoitava Nenäsumute Dekspantenoli 25 ml EUDAMED
- Device Name
- Apteekki Hoitava Nenäsumute Dekspantenoli EUDAMED
- Model / Reference
- 9289816 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06418086102374 EUDAMED
- Basic UDI-DI
- B-06418086102374 EUDAMED
- EMDN Code
- Q030199 NASOPHARYNGEAL DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Finland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Apteekki Hoitava Nenäsumute Dekspantenoli 25 ml by Galena Pharma Oy — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06418086102374 | Class I | Active |
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Manufacturer
- Manufacturer
- Galena Pharma Oy
- EUDAMED SRN
- FI-MF-000000588
Sources (1)
- EUDAMED 4caff235-a3a0-443e-80f5-3c11ba447e3c 61 fields · synced Jul 9, 2026