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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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IBox Touch Compact — 8 UDI-DI variants, MDR (meso international GmbH)

MD Atlas
meso international GmbH

Data from EUDAMED, last updated May 23, 2026

IBox Touch Compact

426033676-IBox1-87

8 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: meso international GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426033676-IBox1-87
Device name: IBox Touch Compact
Device model: IBoxTC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: meso international GmbH
SRN: DE-MF-000006355
Country: Germany
Email: info@meso.biz
Phone: +49 3727 9697 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G86A9CRCSJT1FVBXRZZ8T1CT

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

IBoxTC04260336762010
IBox4K04260336762300
IB4C04260336762409
IB4C4H04260336762485
IB4C4S04260336762478
IB4P04260336762416
IB4P4H04260336762508
IB4P4S04260336762492