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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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TOMTAR MR-LG — 10 UDI-DI variants, MDR (DIETZ GmbH)

MD Atlas
DIETZ GmbH

Data from EUDAMED, last updated May 23, 2026

TOMTAR MR-LG

42602416811MRS00008BC

10 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: DIETZ GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42602416811MRS00008BC
Device name: TOMTAR MR-LG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: DIETZ GmbH
SRN: DE-MF-000009121
Country: Germany
Email: info@dietz-group.de
Phone: +49 7248 9186 0

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H07YXCJ4KMHPDGD6347QR1YD

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

10903904260241689648
10913904260241689693
10904204260241689655
10914204260241689709
10904504260241689662
10914504260241689716
10904804260241689679
10914804260241689723
10905104260241689686
10915104260241689730