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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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Sleeve (including Anchor pin sleeve) — 7 UDI-DI variants, MDR

MD Atlas
EUROTEKNIKA

Data from EUDAMED, last updated May 19, 2026

Sleeve (including Anchor pin sleeve)

37009775bague8J

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: 37009775bague8J
Device name: Sleeve (including Anchor pin sleeve)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 3, 2025

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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Export results

Applied filters

basicUdiUlid01HGXCNPNEPBPQV9B733Y53GCP

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

CGS_TE.22-1003700977506952
UGC_TE_RP03700977510997
CGC_TA30.11003700977507072
CGC_TG03700977507065
UGC_TSI48.10003700977513035
UGC_TE_WP03700977512601
UGC_TE_WP-1003700977511024