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SYNAPTIQ TECHNOLOGIES SRL

Romania RO-MF-000038617 Last updated 21 Oct 2026

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Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

  • Mediq Ref v1.0.0

    Class I EUDAMED Active
  • Mediq RT Ref Mediq RT

    Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV Rheinland LGA Products GmbH 0197 1 certificate

  • HZ 2447216-1 Issued

    Quality management system EU MDR

    Issued
    1 Apr 2026
    Expires
    31 Mar 2031

About

Discover Mediq RT, a platform using AI for organs at risk and lymph nodes auto-contouring as part of radiotherapy treatment planning. Find out more!

From the manufacturer's own website. Source

What SYNAPTIQ TECHNOLOGIES SRL makes

Synaptiq Technologies SRL manufactures radiotherapy treatment planning software, including the Mediq and Mediq RT platforms. These tools incorporate artificial intelligence to automate the contouring of organs at risk and lymph nodes, supporting precision in radiation therapy workflows.

The company’s devices are classified as Class I and Class IIa under EU regulations and are listed in the EUDAMED database. Synaptiq Technologies SRL is based in Romania.

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 Synaptiq Technologies SRL manufacture?

Synaptiq Technologies SRL develops radiotherapy treatment planning software, specifically the Mediq and Mediq RT platforms. These tools use artificial intelligence to automate the contouring of organs at risk and lymph nodes, which helps improve precision and efficiency in radiation therapy planning.

Where is Synaptiq Technologies SRL based?

Synaptiq Technologies SRL is based in Romania, as indicated in its regulatory information.

Which regulatory registries list Synaptiq Technologies SRL’s devices?

Synaptiq Technologies SRL’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This listing ensures transparency and compliance with EU regulatory requirements.

How are Synaptiq Technologies SRL’s devices classified under EU regulations?

Synaptiq Technologies SRL’s devices are classified as Class I and Class IIa under EU medical device regulations. The classification depends on factors like the device’s intended purpose, risk level, and interaction with the patient, with Class IIa indicating a moderate risk requiring additional scrutiny.

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

Information

Country
Romania
Address
23a, Clinicilor, Cluj-Napoca, Romania
Website
synaptiq.io
PRRC contact
Andreea-Maria Mitrofan
EUDAMED SRN
RO-MF-000038617