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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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Patch Test Units — 3 UDI-DI variants, MDR

MD Atlas
Chemotechnique MB Diagnostics AB

Data from EUDAMED, last updated May 30, 2026

Patch Test Units

7340009140025Y

3 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: Chemotechnique MB Diagnostics AB

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 7340009140025Y
Device name: Patch Test Units
Device model: Chemotechnique Patch Test Units
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Chemotechnique MB Diagnostics AB
SRN: SE-MF-000007760
Country: Sweden
Email: info@chemotechnique.se
Phone: +46 40 466 077

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHKP6N1CKECVM96CYTVWNJD

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

BasIQ Ultra07340009140134
IQ Ultimate07340009140011
IQ Ultra07340009140028