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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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opt-on — 2 UDI-DI variants, MDR (orangedental GmbH & Co. KG)

MD Atlas
orangedental GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

opt-on

426037569lup0499000CG

2 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: orangedental GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426037569lup0499000CG
Device name: opt-on
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 20, 2021

Manufacturer & authorised representative

Manufacturer

Name: orangedental GmbH & Co. KG
SRN: DE-MF-000006152
Country: Germany
Email: info@orangedental.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FJE32FTEM1PR7V19FVD116EV

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

4260375690091 / lup049900004260375690091
4260375690107 / lup049910004260375690107