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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

Egosan Underpads cm 60x90 Extra — Class I MDR by Santex S.p.A.

MD Atlas
Santex S.p.A.

EUDAMED last updated this device on May 27, 2026

Egosan Underpads cm 60x90 Extra

8011809TraverseUV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Santex S.p.A.
UDI-DI code: 08011809999954
Reference / catalog number: XT260090C-3

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View device family (Basic UDI)

Manufacturer information

Organization name: Santex S.p.A.
SRN: IT-MF-000010188
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

MDR 00155-AIssued
Quality management systemNotified body: 0476Expiry: Jun 17, 2030

Critical warnings

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

CW009
Do not re-use

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Market distribution

Primary placement in Italy; available across 3 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Belgium		Still on market
Lithuania		Still on market

Device identification

Trade name: Egosan Underpads cm 60x90 Extra
UDI-DI code: 08011809999954
Basic UDI-DI: 8011809TraverseUV
Reference / catalog number: XT260090C-3
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: 3
Additional product description: —
Additional information URL: https://www.santex.itwww.egosan-inco.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08011809999954

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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