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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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ODOFIN Duft Quartett — 2 UDI-DI variants, MDR

MD Atlas
Burghart Messtechnik GmbH

Data from EUDAMED, last updated May 23, 2026

ODOFIN Duft Quartett

426067624DQS6

2 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: Burghart Messtechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426067624DQS6
Device name: ODOFIN Duft Quartett
Device model: ODOFIN Sniffin Sticks
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Burghart Messtechnik GmbH
SRN: DE-MF-000011542
Country: Germany
Email: info@burghart-mt.de
Phone: +494103800760

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GW267FRA0K9JJCKQWRESJWFK

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

LA-13-0006742606762402098
LA-13-0047842606762403392