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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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Alfa R — 5 UDI-DI variants, MDR (BAARS ET ASSOCIES)

MD Atlas
BAARS ET ASSOCIES

Data from EUDAMED, last updated May 19, 2026

Alfa R

3701295AlfaR4B

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: BAARS ET ASSOCIES

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3701295AlfaR4B
Device name: Alfa R
Device model: Alfa R
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: BAARS ET ASSOCIES
SRN: FR-MF-000025734
Country: France
Email: marcantoine@baars-eyewear.com
Phone: 0637545276

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K8QC2PZ1E3JHSQGV9852M0CX

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

AR - C26(01)370129530771
AR - C31(01)370129530769
AR - C36(01)3701295307689
AR - C37(01)370129530767
AR - C39(01)3701295307702