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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

UCGE — Class IIa MDR by Albino Dias de Andrade,…

MD Atlas
Albino Dias de Andrade, S.A.

EUDAMED last updated this device on May 29, 2026

UCGE

560082989C0104XH

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Albino Dias de Andrade, S.A.
UDI-DI code: 05600846267978
Reference / catalog number: 96170545450821.1

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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: UCGE
UDI-DI code: 05600846267978
Basic UDI-DI: 560082989C0104XH
Reference / catalog number: 96170545450821.1
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: UCGE
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)05600846267978

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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.

M0201020201COTTON GAUZES, FOLDED, WITH X-RAY DETECTABLE THREAD, 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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