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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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EC-12S V6 — 6 UDI-DI variants, MDR

MD Atlas
LABTECH Kereskedelmi és Mérnöki Szolgáltató Korlátolt Felelősségű Társaság.

Data from EUDAMED, last updated May 24, 2026

EC-12S V6

5999883490ECGSRY

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: LABTECH Kereskedelmi és Mérnöki Szolgáltató Korlátolt Felelősségű Társaság.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 5999883490ECGSRY
Device name: EC-12S V6
Device model: EC-12S V6
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: LABTECH Kereskedelmi és Mérnöki Szolgáltató Korlátolt Felelősségű Társaság.
SRN: HU-MF-000002846
Country: Hungary
Email: info@labtech.hu
Phone: +36 52 500 128

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K0XSN8J2QBW1SV4CC7C6P573

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

EC-12R V605999883490242
EC-12R/S V605999883490266
EC-12RM V605999883490273
EC-12S V6 05999883490259
EC-3R/S V605999883490297
EC-3S V605999883490280