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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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Protecteur pour pieds (ampoules, cors,… — 8 UDI-DI variants, MDR

MD Atlas
La Brosse et Dupont

Data from EUDAMED, last updated May 19, 2026

Protecteur pour pieds (ampoules, cors, oignons et durillons)

303144PRO761IONY3

8 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: 303144PRO761IONY3
Device name: Protecteur pour pieds (ampoules, cors, oignons et durillons)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KNS22K735WPPKJ4GG9STG4YM

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

31120403031443112040
31120203031443112026
31126203031443112620
31122303031443112231
31123403031443112347
31122003031443112200
31121203031443112125
31120003031443112002