Identity
- Trade Name
- Rollbord Hightec Standard EUDAMED
- Device Name
- Rollbord Hightec EUDAMED
- Model / Reference
- Hightec EUDAMED440.0100 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640144460013 EUDAMED
- Basic UDI-DI
- 764014446RbHT4400000LF EUDAMED
- Direct Marketing DI
- 07640144460013 EUDAMED
- EMDN Code
- V080504 PATIENT TRANSFER BOARDS AND TABLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Rollbord Hightec Standard by Samarit Medical AG — 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 | 764014446RbHT4400000LF | Class I | Active |
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Manufacturer
- Manufacturer
- Samarit Medical AG
- EUDAMED SRN
- CH-MF-000016280
- Authorised Representative
- Samarit Medical Produkt GmbH DE-AR-000014694
Sources (1)
- EUDAMED c86e7ed1-b407-48a0-8eb4-676702fa877f 61 fields · synced Jul 27, 2026