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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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exeol GTA 2% — 2 UDI-DI variants, MDR (SODEL)

MD Atlas
SODEL

Data from EUDAMED, last updated May 19, 2026

exeol GTA 2%

326824F3313-01WE

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: SODEL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 326824F3313-01WE
Device name: exeol GTA 2%
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: SODEL
SRN: FR-MF-000000367
Country: France
Email: info@sodel-sa.eu

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HR7Q5YPJE2EA396BRRT51XVK

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

EXS0092Z103268240055458
EXS0092MLB03268240059258