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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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Liquid Expansion Thermometers — 6 UDI-DI variants, MDR

MD Atlas
Geratherm Medical GERMANY GmbH

Data from EUDAMED, last updated May 23, 2026

Liquid Expansion Thermometers

4018674GTCGT01S8

6 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: Geratherm Medical GERMANY GmbH

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 4018674GTCGT01S8
Device name: Liquid Expansion Thermometers
Device model: GT-1000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: Geratherm Medical GERMANY GmbH
SRN: DE-MF-000007307
Country: Germany
Email: info@geratherm.com
Phone: +4936205980

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JCFSKRPQ43KDYHR7VTPGXGQR

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

GT001001E04018674001014
GT063001E04018674063012
GT068001E04018674068017
GT036001E04018674036016
GT073001E04018674073011
GT069001E04018674069014