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meinHOLTZ Lässig

EUDAMED

Class I (EU MDR)

Ref MH-L02

by Transatlantic HG Stolpe & Co. mbH

Identity

Trade Name
meinHOLTZ Lässig EUDAMED
Device Name
Patiententransporthilfe Rutschbrett EUDAMED
Model / Reference
MH-L02 EUDAMED

Identifiers

Primary DI / UDI-DI
04050856041968 EUDAMED
Basic UDI-DI
4050856TRBD5 EUDAMED
Direct Marketing DI
04050856041968 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

meinHOLTZ Lässig by Transatlantic HG Stolpe & Co. mbH — 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

EUDAMED SRN
DE-MF-000009432

Sources (1)

  • EUDAMED e66fd08d-eac3-4d8b-a999-35c7f3303382 61 fields · synced Jul 19, 2026