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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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Extractor — 11 UDI-DI variants, MDR (EUROTEKNIKA)

MD Atlas
EUROTEKNIKA

Data from EUDAMED, last updated May 19, 2026

Extractor

37009775extracteurZQ

11 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: EUROTEKNIKA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37009775extracteurZQ
Device name: Extractor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: EUROTEKNIKA
SRN: FR-MF-000004032
Country: France
Email: qualite-sallanches@lyra.dental
Phone: +33176420060

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HKV15G8DB412A0X6KG9A8FEN

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

CEP_16.17503700977507461
CEP_16.20503700977512823
CEP_18.17503700977507454
CEP_14.20503700977512816
CCK_QI15.15003700977507836
CEP_18.20503700977512830
CEP_14.17503700977507478
CCK_QV15.15003700977507829
CEP_20.20503700977512847
CEP_20.17503700977507447
CCK_QH15.15003700977512083