← Back to catalogue

Rollboard Vision rot

EUDAMED

Class I (EU MDR)

Ref PMF-9095

by Petermann GmbH

Identity

Trade Name
Rollboard Vision rot EUDAMED
Device Name
Rollboard EUDAMED
Model / Reference
PMF-9095 EUDAMED

Identifiers

Primary DI / UDI-DI
04250355394958 EUDAMED
Basic UDI-DI
42503553KROL019191868Q EUDAMED
Direct Marketing DI
04250355394958 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

Rollboard Vision rot by Petermann GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Petermann GmbH
EUDAMED SRN
DE-MF-000013598

Sources (1)

  • EUDAMED a715d296-0cc4-4a23-93da-074bb48fa35f 61 fields · synced Jun 19, 2026