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Rollbord Hightec Surgiboard

EUDAMED

Class I (EU MDR)

Ref 440.0400Model Hightec

by Samarit Medical AG

Identity

Trade Name
Rollbord Hightec Surgiboard EUDAMED
Device Name
Rollbord Hightec EUDAMED
Model / Reference
Hightec EUDAMED
440.0400 EUDAMED

Identifiers

Primary DI / UDI-DI
07640144460044 EUDAMED
Basic UDI-DI
764014446RbHT4400000LF EUDAMED
Direct Marketing DI
07640144460044 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

Category: Patient lifting system stretcher

Rollbord Hightec Surgiboard by Samarit Medical AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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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 a01f2f37-ccae-4c32-aeea-18f8f5c36785 61 fields · synced Jul 29, 2026