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G-Squared SRL

Italy IT-MF-000016857 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • EyeRad Ref EyeRad 3.1

    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)

TUV Rheinland Italia SRL 1936 1 certificate

  • ITH 1344197 1 Supplemented

    Quality management system EU MDR

    Issued
    14 Jul 2026
    Expires
    8 Aug 2028
    Reason
    Other

Notified bodies

About

Copyright © 2026 - G-Squared - Registered office: Via F. Baracca, 204 - 36100 Vicenza - VAT 03448720247 - REA VI-326450

Translated from the manufacturer's own website. Source

What G-Squared SRL makes

G-Squared SRL manufactures the EyeRad, a handheld ophthalmic imaging device designed for retinal examination and diagnostic imaging. This device is intended for capturing detailed images of the retina to assist in the detection and monitoring of retinal conditions.

The EyeRad is classified as a Class IIa medical device and is listed in the EU’s eudamed registry. The company is based in Italy.

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 G-Squared SRL manufacture?

G-Squared SRL manufactures the EyeRad, a handheld ophthalmic imaging device. This device is specifically designed for retinal examination and diagnostic imaging, enabling detailed capture of retinal images to aid in detecting and monitoring retinal conditions.

Where is G-Squared SRL based?

G-Squared SRL is based in Italy, with its registered office located in Vicenza. The company’s headquarters and operational presence are centered around this region.

Which regulatory registries list G-Squared SRL’s devices?

G-Squared SRL’s devices, including the EyeRad, are listed in the EU’s eudamed registry. This registry is used to track medical devices authorized for placement on the European market under applicable regulations.

How are G-Squared SRL’s devices classified?

The EyeRad, G-Squared SRL’s primary device, is classified as a Class IIa medical device. This classification is determined based on its intended purpose and associated risk level, requiring compliance with specific regulatory requirements to ensure safety and performance.

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

Information

Country
Italy
Address
204, VIA FRANCESCO BARACCA, VICENZA, Italy
Phone
+3904441497266
PRRC contact
Cristina Gatto
EUDAMED SRN
IT-MF-000016857