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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

10.642/I/424510 — Class I MDR by Moritz Reha-Hilfen GmbH

MD Atlas
Moritz Reha-Hilfen GmbH

EUDAMED last updated this device on Apr 4, 2026

10.642/I/424510

426072775004A6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Moritz Reha-Hilfen GmbH
UDI-DI code: 04255942206317
Reference / catalog number: 10.642/I/424510

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Manufacturer information

Organization name: Moritz Reha-Hilfen GmbH
SRN: DE-MF-000005119
Manufacturer status: Active

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10.804/07426072775006AAOn the market 10.804/03426072775006AAOn the market 10.774/17426072775005A8On the market 10.774/07426072775005A8On the market 10.674-ST426072775003A4On the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Innenkern enthält Latex. Nicht anwenden bei einer Latexallergie.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04255942206317
Basic UDI-DI: 426072775004A6
Reference / catalog number: 10.642/I/424510
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Latexkissen, Stiftlatex, Inko-Bezug REF7072, 42x45x10cm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.