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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 suction unit disinfectant — 1 UDI-DI variant, MDR

MD Atlas
United Disinfectant Manufacturers AG

Data from EUDAMED, last updated May 31, 2026

Dental suction unit disinfectant

955102414018ALQF

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: United Disinfectant Manufacturers AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 955102414018ALQF
Device name: Dental suction unit disinfectant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: United Disinfectant Manufacturers AG
SRN: LI-MF-000036153
Country: Liechtenstein
Email: info@udm.li

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSSPXFF01JYBX8W57R2K49NH

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

CH-07102009551024142661