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

MD Atlas
BAARS ET ASSOCIES

Data from EUDAMED, last updated May 19, 2026

Alfa X

3701295AlfaX4P

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: 3701295AlfaX4P
Device name: Alfa X
Device model: Alfa X
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

basicUdiUlid01K8QDSD54NEYD79A62VAVX47Z

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

AX - C23(01)3701295311754
AX - C26(01)3701295312256
AX - C43(01)3701295312232
AX - C44(01)3701295312249
AX - C45(01)3701295312225