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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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DENTAL INSTRUMENTS — 217 UDI-DI variants, MDR

MD Atlas
BADER EUROPE GROUP S.L.

Data from EUDAMED, last updated May 23, 2026

DENTAL INSTRUMENTS

8437027932INSTRUM3K

217 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: BADER EUROPE GROUP S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437027932INSTRUM3K
Device name: DENTAL INSTRUMENTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: BADER EUROPE GROUP S.L.
SRN: ES-MF-000041884
Country: Spain
Email: gabriel@bader.es

Variants by status

UDI-DI variants

217 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J29DKAQNJBNPAJ8JVW5NFABM

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

5/36808435783606774
17/405208435783606033
123708437027932847
17/4002208435783604992
B13008435783607603
17/4042-208435783605920
17/4006-408435783605135
17/4036-108435783605838
10/02008437027932182
121208437027932656
B18008435783607641
17/4006-708435783605166
17/4004-308435783605043
122608437027932762
061000708435783600727
17/4001808435783604985
5/059808435783606729

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