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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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Pansement adhésif — 13 UDI-DI variants, MDR (La Brosse et Dupont)

MD Atlas
La Brosse et Dupont

Data from EUDAMED, last updated May 19, 2026

Pansement adhésif

303144PAN546ENTLP

13 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: La Brosse et Dupont

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 303144PAN546ENTLP
Device name: Pansement adhésif
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: La Brosse et Dupont
SRN: FR-MF-000004610
Country: France
Email: matthieubernard@labrosseetdupont.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH10J18HRFR5D54ZQAJF8XP7

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

31201903031443120199
31203503031443120359
31202003031443120205
31202803031443120281
31205403031443120540
31203303031443120335
31202503031443120250
31201303031443120137
31201603031443120168
31202203031443120229
31202303031443120236
31203003031443120304
31201003031443120106