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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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GlucoTab — 6 UDI-DI variants, MDR (decide Clinical Software GmbH)

MD Atlas
decide Clinical Software GmbH

Data from EUDAMED, last updated May 23, 2026

GlucoTab

918000023GT20-11AQG

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: decide Clinical Software GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 918000023GT20-11AQG
Device name: GlucoTab
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Oct 21, 2021

Manufacturer & authorised representative

Manufacturer

Name: decide Clinical Software GmbH
SRN: AT-MF-000001001
Country: Austria
Email: office@decide-clinical.com
Phone: +43 316 318551

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJHKZ7QEM68H5WCAZKGWMSTR

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

GlucoTab R10.009180000230063
GlucoTab R10.109180000230070
GlucoTab R8.009180000230025
GlucoTab R8.109180000230032
GlucoTab R9.009180000230049
GlucoTab R9.109180000230056