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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 restorative devices — 1,159 UDI-DI variants, MDR

MD Atlas
pritidenta GmbH

Data from EUDAMED, last updated May 23, 2026

Dental restorative devices

42513669ZRO2RQ

1,159 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: pritidenta GmbH

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 42513669ZRO2RQ
Device name: Dental restorative devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: pritidenta GmbH
SRN: DE-MF-000006241
Country: Germany
Email: info@pritidenta.com

Variants by status

UDI-DI variants

1,159 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRGCJC19KYDA8PRHSA8FHHM0

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

13107-D985-10A2T04251366902705
13107-D985-14C1T04251366903405
13107-D985-14C2T04251366903412
13107-D985-18B2T04251366903214
13107-D985-20BLT04251366903986
13107-D985-20A3T04251366902972
13107-D985-30D3T04251366911479
13107-D985-30ADT04251366911073
13107-D985-25A4T04251366903030