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Qp-059180-R

EUDAMED

Class I (EU MDR)

Ref QP-059180-RModel QP-059150-R

by GBUK Group

Identity

Model / Reference
QP-059150-R EUDAMED
QP-059180-R EUDAMED

Identifiers

Primary DI / UDI-DI
05060405744638 EUDAMED
Basic UDI-DI
506040574TransferBoardsL4 EUDAMED
Direct Marketing DI
05060405744638 EUDAMED
EMDN Code
V080504 PATIENT TRANSFER BOARDS AND TABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Qp-059180-R by GBUK Group — 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
GBUK Group
EUDAMED SRN
GB-MF-000002238
Authorised Representative
Qualrep Services B.V. NL-AR-000000537

Sources (1)

  • EUDAMED b79c4d84-197e-444b-a0a0-06815ac89a51 61 fields · synced Jun 18, 2026