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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

110244433 — Class I MDR by Werkmeister GmbH + Co. KG

MD Atlas
Werkmeister GmbH + Co. KG

EUDAMED last updated this device on Sep 11, 2025

110244433

4048486113901YX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Werkmeister GmbH + Co. KG
UDI-DI code: 04048486052737
Reference / catalog number: 110244433

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Manufacturer information

Organization name: Werkmeister GmbH + Co. KG
SRN: DE-MF-000005120
Manufacturer status: Active

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3076/STÜCK4048486110301XCOn the market 3075/STÜCK4048486110301XCOn the market 160140408RE40484862646012WOn the market 160144442RE40484862646012WOn the market 160144442LI40484862646012WOn the market

Critical warnings

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

CW011
Bedingt geeignet bei Dekubitus im fortgeschrittenem Stadium.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04048486052737
Basic UDI-DI: 4048486113901YX
Reference / catalog number: 110244433
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: PneumoKiss Kaltschaumkissen B44xT43x3Hcm RG40 Marine HMV: 11.11.01.3083
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.