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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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Electro-gel — 4 UDI-DI variants, MDR (Telic, S.A.U.)

MD Atlas
Telic, S.A.U.

Data from EUDAMED, last updated May 23, 2026

Electro-gel

8427734ECGGELVB

4 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: Telic, S.A.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8427734ECGGELVB
Device name: Electro-gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Telic, S.A.U.
SRN: ES-MF-000001853
Country: Spain
Email: info@telic.es
Phone: 00 34 93 865 61 25

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J4K6JPQ2DEBTE05Z4BZE3PRQ

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

60204707640109604322
3G250EC03663996018724
G-1008427734001899
PF010603760316090092