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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-S — 10 UDI-DI variants, MDR (DIETZ GmbH)

MD Atlas
DIETZ GmbH

Data from EUDAMED, last updated May 23, 2026

TOMTAR MR-S

42602416811MRS00007BA

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: 42602416811MRS00007BA
Device name: TOMTAR MR-S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

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

basicUdiUlid01H0FK8BCM65WJAKKHV2799S7C

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

10803904260241689549
10813904260241689594
10804204260241689556
10814204260241689600
10804504260241689563
10814504260241689617
10804804260241689570
10814804260241689624
10805104260241689587
10815104260241689631