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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

SPARADRAP PEAU SENSIBLE — Class I MDR by La Brosse et Dupont

MD Atlas
La Brosse et Dupont

EUDAMED last updated this device on May 21, 2026

SPARADRAP PEAU SENSIBLE

303144SPA362RAPQE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: La Brosse et Dupont
UDI-DI code: 03031443121011
Reference / catalog number: 312101

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Manufacturer information

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

Critical warnings

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

CW009
Usage unique. Risque d’infection croisée et d’efficacité réduite en cas de réutilisation.
CW083
Ne pas utiliser en cas de sensibilité aux adhésifs
CW011
Ne pas utiliser pour des plaies infectées et des brûlures

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: SPARADRAP PEAU SENSIBLE
UDI-DI code: 03031443121011
Basic UDI-DI: 303144SPA362RAPQE
Reference / catalog number: 312101
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)

M050101PLASTERS ON SPOOLS (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

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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.