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Organization name
UDI-DI code
Reference / catalog number

2265027 — Class I MDR by Igefa Handelsgesellschaf…

MD Atlas
Igefa Handelsgesellschaft mbH & Co. KG

EUDAMED last updated this device on Dec 23, 2025

2265027

4024009210823141T4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Igefa Handelsgesellschaft mbH & Co. KG
UDI-DI code: 04024009008337
Reference / catalog number: 2265027

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Manufacturer information

Organization name: Igefa Handelsgesellschaft mbH & Co. KG
SRN: DE-MF-000029971
Manufacturer status: Active

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: 04024009008337
Basic UDI-DI: 4024009210823141T4
Reference / catalog number: 2265027
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: Krankenunterlage, zur besonders wirtschaftlichen Versorgung, schrankfertig vorgefaltet, hygienisch in Beuteln unterverpackt, besitzt Saugkörper aus rein-weißen, chlorfrei gebleichten Zellstoff-Flocken, durch die Rautenprägung wird Flüssigkeit schnell im Saugkörper verteilt, Rückseite besteht aus einer wasserundurchlässigen Folie, Oberseite besteht aus einem hautfreundlichen, textilähnlichen Vliesmaterial, Breite 60 cm, Farbe blau, Länge 60 cm, Saugleistung (ISO) 880 ml, 1 Beutel à 25 Stk, (Krt à 12 Btl).
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T04010201UNTUCKABLE UNDERPADS

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

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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.