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Rollboard Vision rot

EUDAMED

Class I (EU MDR)

Ref PMF-9180

by Petermann GmbH

Identity

Trade Name
Rollboard Vision rot EUDAMED
Device Name
Rollboard EUDAMED
Model / Reference
PMF-9180 EUDAMED

Identifiers

Primary DI / UDI-DI
04250355394804 EUDAMED
Basic UDI-DI
42503553KROL019191868Q EUDAMED
Direct Marketing DI
04250355394804 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

Rollboard Vision rot by Petermann GmbH — 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
Petermann GmbH
EUDAMED SRN
DE-MF-000013598

Sources (1)

  • EUDAMED 516aafff-337a-47ea-b3fe-e15c544c0d24 61 fields · synced Jun 20, 2026