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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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Class I - Non-sterile devices allowing… — 8 UDI-DI variants, MDR

MD Atlas
Cair LGL

Data from EUDAMED, last updated May 19, 2026

Class I - Non-sterile devices allowing administration to patient

3661657ADM01NSLB

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: Cair LGL

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 3661657ADM01NSLB
Device name: —
Device model: Class I - Non-sterile devices allowing administration to patient
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Cair LGL
SRN: FR-MF-000007921
Country: France
Email: contact@cairlgl.fr
Phone: +33478437744

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJ50074FXGW0YE3V86EZ0FPA

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

BBEI250NS13661657051698
AC03313661657000566
UR140013661657014921
UR143013661657014938
SU20013661657013771
TR5313661657014853
TR10313661657014761
TR3313661657014808