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Apteq Mielikki Limaa irrottava yskähunaja 120 ml FI
EUDAMEDClass IIa (EU MDR)
Ref FTPR44
Identity
- Trade Name
- Apteq Mielikki Limaa irrottava yskähunaja 120 ml FI EUDAMED
- Device Name
- ZERO COUGH FAMILY SYRUP EUDAMED
- Model / Reference
- FTPR44 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08056300620921 EUDAMED
- Basic UDI-DI
- 805630062FTPR449L EUDAMED
- EMDN Code
- V9017 ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Finland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Apteq Mielikki Limaa irrottava yskähunaja 120 ml FI by Labomar S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 805630062FTPR449L | Class IIa | Active |
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Manufacturer
- Manufacturer
- Labomar S.p.A.
- EUDAMED SRN
- IT-MF-000007965
Sources (1)
- EUDAMED 0ce9bbaf-6068-4465-901b-9773a0bdbbff 61 fields · synced Jul 18, 2026