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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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Mona Terminal — 4 UDI-DI variants, MDR (Clinomic Medical GmbH)

MD Atlas
Clinomic Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Mona Terminal

4260735730029B

4 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: Clinomic Medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4260735730029B
Device name: Mona Terminal
Device model: Mona Terminal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Clinomic Medical GmbH
SRN: DE-MF-000013339
Country: Germany
Email: info@clinomic.ai
Phone: +49 241 894 387 37

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JD4MHQF2BN21AAQGMCYP54KF

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

Mona Terminal 1.1 series 0.104260735730009
Mona Terminal 1.1 series 0.304260735730030
Mona Terminal 2.0 series 0.104260735730054
Mona Terminal 1.1 series 0.204260735730023