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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

INTRA COMPRESS — Class I MDR by Albino Dias de Andrade,…

MD Atlas
Albino Dias de Andrade, S.A.

EUDAMED last updated this device on May 29, 2026

INTRA COMPRESS

560082989A0101WM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Albino Dias de Andrade, S.A.
UDI-DI code: 05600846261327
Reference / catalog number: 94300010100400

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View device family (Basic UDI)

Manufacturer information

Organization name: Albino Dias de Andrade, S.A.
SRN: PT-MF-000002823
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

ES25/00000301Supplemented
Quality management systemNotified body: 1639Expiry: Mar 13, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement	Jan 1, 2026	Still on market

Device identification

Trade name: INTRA COMPRESS
UDI-DI code: 05600846261327
Basic UDI-DI: 560082989A0101WM
Reference / catalog number: 94300010100400
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: INTRA COMPRESS
Additional information URL: No additional information URL provided by the manufacturer.
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)05600846261327

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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.

M0202010102NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE

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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