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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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Isolation Device Server II — 4 UDI-DI variants, MDR

MD Atlas
Trium Analysis Online GmbH

Data from EUDAMED, last updated May 23, 2026

Isolation Device Server II

426034662IDS2rev3XP

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: Trium Analysis Online GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426034662IDS2rev3XP
Device name: Isolation Device Server II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Trium Analysis Online GmbH
SRN: DE-MF-000007016
Country: Germany
Email: info@trium.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KR163K7SYE0XENXC7MSY32F8

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

Isolation Device Server Type II04260346620041
Isolation Device Server Type II04260346620058
Isolation Device Server Type II (IDS2)04260346620027
Isolation Device Server Type II (IDS2)04260346620034