Identity
- Device Name
- ASPIFLEX EUDAMED
- Model / Reference
- ASPIFLEX EUDAMEDASP2010 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08055348435016 EUDAMED
- Basic UDI-DI
- 805534843FT04ASPCY EUDAMED
- EMDN Code
- A03020199 EXTENSIONS - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
Aspiflex by Meika Group S.r.l. — 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 | 805534843FT04ASPCY | Class IIa | Active |
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Manufacturer
- Manufacturer
- Meika Group S.r.l.
- EUDAMED SRN
- IT-MF-000029106
Sources (1)
- EUDAMED 02a682b9-e081-4c2e-a2c4-c45444f79ffd 61 fields · synced Jun 19, 2026