Identity
- Device Name
- S91020200.0 EUDAMED
- Model / Reference
- PROLEX EUDAMEDPROLUNGA SPIRALATA IN PU EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08055348432992 EUDAMED
- Basic UDI-DI
- B-08055348432992 EUDAMED
- EMDN Code
- A03020101 LOW PRESSURE EXTENSION LINES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
A comprehensive overview of the S91020200.0 medical device, including its benefits, features, and regulatory compliance.
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-08055348432992 | Class I | Active |
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Manufacturer
- Manufacturer
- Meika Group S.r.l.
- EUDAMED SRN
- IT-MF-000029106
Sources (1)
- EUDAMED 15106449-19d2-4f28-9aff-cd5b83112743 61 fields · synced Jun 26, 2026