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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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Main Control Device — 3 UDI-DI variants, MDR (ReDent Nova GmbH)

MD Atlas
ReDent Nova GmbH

Data from EUDAMED, last updated May 23, 2026

Main Control Device

426235751MCD001Y3

3 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: ReDent Nova GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426235751MCD001Y3
Device name: Main Control Device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 31, 2025

Manufacturer & authorised representative

Manufacturer

Name: ReDent Nova GmbH
SRN: DE-MF-000032545
Country: Germany
Email: office@redentnova.de
Phone: +49(0)3084430096

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQNSN7HV6W9X194HW75TACH8

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

B-SA-IMC-00-000-000-078404262357510106
B-SA-IMC-00-000-000-083904262357510205
B-SA-IMC-00-000-000-088804262357510212