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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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Fußanlasser — 5 UDI-DI variants, MDR

MD Atlas
Ultradent Dental-Medizinische-Geräte GmbH & Co KG

Data from EUDAMED, last updated May 23, 2026

Fußanlasser

426074666UD733036X

5 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: Ultradent Dental-Medizinische-Geräte GmbH & Co KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426074666UD733036X
Device name: Fußanlasser
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ultradent Dental-Medizinische-Geräte GmbH & Co KG
SRN: DE-MF-000020027
Country: Germany
Email: info@ultradent.de
Phone: 08942099270

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQA3XPGG3RNS44HSY6K4EH9M

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

878704260746660319
878904260746660326
803704260746660302
870004260746660289
802004260746660296