Identity
- Trade Name
- LETTINO EROS EUDAMED
- Device Name
- EROS EUDAMED
- Model / Reference
- SERIE PROFESSIONAL EUDAMED1111F EUDAMED
Identifiers
- Primary DI / UDI-DI
- 80505939404692 EUDAMED80505939404760 EUDAMED
- Basic UDI-DI
- 8050593941111FSE EUDAMED
- Direct Marketing DI
- 80505939404692 EUDAMED80505939404760 EUDAMED
- EMDN Code
- Z12069099 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy 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
Lettino Eros by FISIOTECH srl — Class I — 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 | 8050593941111FSE | Class I | Active |
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Manufacturer
- Manufacturer
- FISIOTECH srl
- EUDAMED SRN
- IT-MF-000028185
Sources (2)
- EUDAMED 9f48043d-5307-4fbe-abe7-6068c0d405de 61 fields · synced Jul 29, 2026
- EUDAMED e76e159b-6b37-4323-a908-70897f40da90 61 fields · synced May 17, 2026