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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 unit Stomadent — 2 UDI-DI variants, MDR (STOMADENT SK s.r.o.)

MD Atlas
STOMADENT SK s.r.o.

Data from EUDAMED, last updated May 31, 2026

Dental unit Stomadent

85820000433DU001JX

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: STOMADENT SK s.r.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 85820000433DU001JX
Device name: Dental unit Stomadent
Device model: Dental unit Stomadent
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: STOMADENT SK s.r.o.
SRN: SK-MF-000031507
Country: Slovakia
Email: stomadent@stomadent.sk
Phone: +421910406473

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KPZNWV7727G5CPM08SDYRB4P

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

Stomadent Impuls85820000433070
Stomadent NEO85820000433148