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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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GEL ECOGRAFIC — 5 UDI-DI variants, MDR (Klintensiv SRL)

MD Atlas
Klintensiv SRL

Data from EUDAMED, last updated May 31, 2026

GEL ECOGRAFIC

5940674714GELECOGRAFIEBA

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: Klintensiv SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5940674714GELECOGRAFIEBA
Device name: GEL ECOGRAFIC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Klintensiv SRL
SRN: RO-MF-000041211
Country: Romania
Email: ra@klintensiv.com
Phone: +40 757 094 266

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JRDXDAPK96NFRP3PKBE2K5F6

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

594908841123805940674714030
594908841119105940674714054
594908841122105940674714023
0594908841124505940674714047
594908841118405940674714016