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Rettungsmulde

EUDAMED

Class I (EU MDR)

Ref 5039Model Rettungsmulde

by B.u.W. Schmidt GmbH

Identity

Trade Name
Rettungsmulde EUDAMED
Rettungsmulde "DGzRS" EUDAMED
Device Name
Rettungsmulde EUDAMED
Model / Reference
Rettungsmulde EUDAMED
5039 EUDAMED

Identifiers

Primary DI / UDI-DI
04250603650393 EUDAMED
Basic UDI-DI
42506036RESQMULDE224UW EUDAMED
Direct Marketing DI
04250603650393 EUDAMED
EMDN Code
V08050199 PATIENT TRANSFER STRETCHERS - OTHER 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

Rettungsmulde by B.u.W. Schmidt 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

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Manufacturer

Manufacturer
B.u.W. Schmidt GmbH
EUDAMED SRN
DE-MF-000022478

Sources (2)

  • EUDAMED cdff7d99-0139-4736-8feb-f8c5c867f4a1 61 fields · synced Jul 24, 2026
  • EUDAMED 1eacfa00-68f5-40d7-be09-b4316f5a09b3 61 fields · synced Jul 24, 2026