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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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Drill guide — 7 UDI-DI variants, MDR (EUROTEKNIKA)

MD Atlas
EUROTEKNIKA

Data from EUDAMED, last updated May 19, 2026

Drill guide

37009775guideDC

7 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: 37009775guideDC
Device name: Drill guide
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 6, 2023

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01HGZJY857XDH0ZSG002HJBKKV

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

CGK_3N03700977507034
CGK_3NS03700977507027
CGK_N.RPWP03700977507003
CGK_NAT03700977506990
CGK_303700977507041
CGK_AEST03700977507010
CGK_U03700977506983