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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 Treatment System Fimet — 5 UDI-DI variants, MDR (Fimet Oy)

MD Atlas
Fimet Oy

Data from EUDAMED, last updated May 23, 2026

Dental Treatment System Fimet

6429810585dentalsystem5A

5 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: Fimet Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 6429810585dentalsystem5A
Device name: Dental Treatment System Fimet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Fimet Oy
SRN: FI-MF-000006831
Country: Finland
Email: fimet@fimet.fi
Phone: +358 19 521 6600

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HM620KR2Q6MV8SMDN58XZPKA

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

F1 Arcus06429810585042
NEO06429810585059
NEO CART06429810585097
NEO CEILING06429810585103
NEO City06429810585080