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Organization name
UDI-DI code
Reference / catalog number

Isolation Device Server Type II… — Class I MDR

MD Atlas
Trium Analysis Online GmbH

EUDAMED last updated this device on May 12, 2026

Isolation Device Server Type II (IDS2)

426034662IDS2rev3XP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Trium Analysis Online GmbH
UDI-DI code: 04260346620034
Reference / catalog number: 1002Z-IDS-02-UK

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Manufacturer information

Organization name: Trium Analysis Online GmbH
SRN: DE-MF-000007016
Manufacturer status: Active

Related devices

Isolation Device Server Type II426034662IDS2rev3XPOn the market Isolation Device Server Type II426034662IDS2rev3XPOn the market Isolation Device Server Type II (IDS2)426034662IDS2rev3XPOn the market 002001E-02-4426034662TriumCTGOnlineQUOn the market 002001C-05426034662TriumCTGOnlineQUOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

10 warnings recorded — scroll inside the panel to see all entries.

CW999
The IDS2 should not be used adjacent to, or stacked with, other equipment. If adja- cent or stacked use is necessary, the IDS2 should be tested to verify normal operation in the con- figuration in which it is being used.
CW999
Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the IDS2, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.
CW999
Wrong polarity can damage the device! Pay attention to polarity - / +.
CW999
Prevent shock-hazard: Never use an IDS2/power supply with damaged housing or ca- ble.
CW999
Danger of fatal shock: Use IDS2 in dry environment only. Avoid splashing water. Do not immense in liquids!
CW999
Only use original spare parts or accessories.
CW999
For separating the connection always pull on the plug, never the cable.
CW999
Do not connect the IDS2 to a telephone outlet. Use this device only attached to an Ethernet computer network.
CW999
Do not modify this equipment without authorization of the manufacturer.
CW999
Accessory equipment or cables not in accordance with this instructions may cause either harmful electromagnetic interference or result in a reduced protection of the device. It is possible that radio-frequency transmitting equipment in close proximity may result in disruption of performance of this device. The operator is encouraged to determine the electromagnetic compatibility before this equipment is used for the first time.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Isolation Device Server Type II (IDS2)
UDI-DI code: 04260346620034
Basic UDI-DI: 426034662IDS2rev3XP
Reference / catalog number: 1002Z-IDS-02-UK
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The Isolation Device Server Type 2 (IDS2) is a serial device server which provides a medical grade galvanic insulation. This simplifies the integration into the patient vicinity and is a distinguishing fea - ture compared to competitors.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080180PRENATAL DIAGNOSTIC INSTRUMENTS - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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