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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

311212 — Class I MDR by La Brosse et Dupont

MD Atlas
La Brosse et Dupont

EUDAMED last updated this device on Apr 9, 2026

311212

303144PRO761IONY3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: La Brosse et Dupont
UDI-DI code: 03031443112125
Reference / catalog number: 311212

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Manufacturer information

Organization name: La Brosse et Dupont
SRN: FR-MF-000004610
Manufacturer status: Active

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.

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW011
Usage externe uniquement. Tenir hors de portée des enfants. Ne pas utiliser sur une plaie ou sur peau infectée.
CW083
Ne pas utiliser en cas d'allergie connue au latex.
CW009
Usage unique. Risque de contamination et réduction de performance en cas de réutilisation.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03031443112125
Basic UDI-DI: 303144PRO761IONY3
Reference / catalog number: 311212
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03030203FOAM PADS

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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