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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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optiprint durotec — 4 UDI-DI variants, MDR (dentona AG)

MD Atlas
dentona AG

Data from EUDAMED, last updated May 23, 2026

optiprint durotec

426067016durotec5B

4 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: dentona AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426067016durotec5B
Device name: optiprint durotec
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: dentona AG
SRN: DE-MF-000005550
Country: Germany
Email: mailbox@dentona.de
Phone: +49 (0) 231 555 6 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KF0W86SW2VW1Z7AJJJWP3XET

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

4846104260670161425
4846004260670161418
4847004260670161432
4847104260670161449