← Back to catalogue

meinHOLTZ Original

EUDAMED

Class I (EU MDR)

Ref MH-O01

by Transatlantic HG Stolpe & Co. mbH

Identity

Trade Name
meinHOLTZ Original EUDAMED
Device Name
Patiententransporthilfe Rutschbrett EUDAMED
Model / Reference
MH-O01 EUDAMED

Identifiers

Primary DI / UDI-DI
04050856044969 EUDAMED
Basic UDI-DI
4050856TRBD5 EUDAMED
Direct Marketing DI
04050856044969 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

meinHOLTZ Original by Transatlantic HG Stolpe & Co. mbH — 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

EUDAMED SRN
DE-MF-000009432

Sources (1)

  • EUDAMED 9def2d90-054c-4bed-bd68-7bc93af11e99 61 fields · synced Jun 18, 2026