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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

10 G OF COTTON PELLETS N°4 — Class I MDR by Alan & Co

MD Atlas
Alan & Co

EUDAMED last updated this device on Nov 24, 2025

10 G OF COTTON PELLETS N°4

542503254CRA020UE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Alan & Co
UDI-DI code: 05425032541935
Reference / catalog number: CPA4 10G

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Manufacturer information

Organization name: Alan & Co
SRN: BE-MF-000000141
Manufacturer status: Active

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4 GR COTTON PELLETS N°3542503254CRA020UEOn the market BRAIDED RETRACTION CORDS N° 0542503254RCA011VBOn the market BRAIDED RETRACTION CORDS N° 00542503254RCA011VBOn the market CARRES DE COTON 10 X 10 CM542503254PADS0324ROn the market CARRES DE COTON 5 X 5 CM542503254PADS0324ROn the market

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	Nov 24, 2025	Dec 31, 2099

Device identification

Trade name: 10 G OF COTTON PELLETS N°4
UDI-DI code: 05425032541935
Basic UDI-DI: 542503254CRA020UE
Reference / catalog number: CPA4 10G
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: BOXES OF 10 G OF COTTON PELLETS ALAN N°4 - XS
Additional information URL: https://www.alanmedical.be/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q019004DENTAL COTTON ROLLS

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.