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Triton Electronic Systems Ltd

Russia RU-MF-000015915 Last updated 21 Oct 2026

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Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

Authorised representatives

About

Manufacture and sale of medical equipment, OEM solutions. A company operating in the market of development, production, sale and maintenance of medical resuscitation equipment.

Translated from the manufacturer's own website. Source

What Triton Electronic Systems Ltd makes

Triton Electronic Systems Ltd produces mechanical ventilators for intensive care, including the Zisline MV200, MV300, and MV350 models, designed for respiratory support in critical care settings. The company also manufactures depth of anaesthesia and sedation monitors, such as the MGA-06, which assist in monitoring patient sedation levels during medical procedures.

These devices fall under Class IIb classification in the EU regulatory framework and are listed in the eudamed database. The company is based in Russia.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Triton Electronic Systems Ltd manufacture?

Triton Electronic Systems Ltd specialises in critical care and anaesthesia monitoring equipment. The company produces mechanical ventilators, such as the Zisline MV200, MV300, and MV350, which provide respiratory support in intensive care settings. Additionally, they manufacture depth of anaesthesia and sedation monitors, like the MGA-06, which help clinicians monitor patient sedation levels during medical procedures.

Where is Triton Electronic Systems Ltd based?

Triton Electronic Systems Ltd is headquartered in Russia. The company’s location influences its regulatory compliance requirements, particularly for devices marketed in the EU or other jurisdictions with specific geographic regulations.

Which regulatory registries list Triton Electronic Systems Ltd’s devices?

Triton Electronic Systems Ltd’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and traceability for devices authorised under EU regulations, such as those classified under Class IIb.

How are Triton Electronic Systems Ltd’s devices classified under EU regulations?

Triton Electronic Systems Ltd’s devices, including ventilators and anaesthesia monitors, fall under Class IIb classification in the EU. This classification is assigned based on risk assessment criteria—Class IIb devices pose moderate to high risks and require additional scrutiny, such as conformity assessments and technical documentation reviews, to ensure safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Russia
Address
33, Bajova street, Ekaterinburg, Russia
Phone
+7 343 304 60 50
PRRC contact
Vladimir Polunin
EUDAMED SRN
RU-MF-000015915