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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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Plage braille b.note 20 cellules — 5 UDI-DI variants, MDR (BELVUE)

MD Atlas
BELVUE

Data from EUDAMED, last updated May 19, 2026

Plage braille b.note 20 cellules

3770022624ebdisplays79

5 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: BELVUE

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770022624ebdisplays79
Device name: Plage braille b.note 20 cellules
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: BELVUE
SRN: FR-MF-000009482
Country: France
Email: gestion@eurobraille.fr
Phone: +33155269100

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FZFPXSSEMM1HKZ5SQZR087NS

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

b.note 2003770022624009
b.note 4003770022624016
b.note 40 light03770022624023
esys 6403770022624030
esys 8003770022624047