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TECHNOLOGY S.R.L.

Italy IT-MF-000035728 Last updated 17 Sep 2026

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Devices
22
Registries
EUDAMED
FDA recalls
0

Catalogue22

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EUDAMED certificates1

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

EUDAMED certificates (1)

BUREAU VERITAS ITALIA S.P.A. 1370 1 certificate

  • IT344983 Supplemented

    Quality management system EU MDR

    Issued
    15 Apr 2026
    Expires
    6 Aug 2030
    Reason
    Add device or group

Related companies

Notified bodies

What TECHNOLOGY S.R.L. makes

Technology S.R.L. manufactures a range of Class IIa medical devices primarily used in diagnostic imaging and radiation therapy. Their portfolio includes devices such as X-ray imaging systems, mammography units, and fluoroscopy equipment, designed for clinical and procedural applications. These products are intended for use in hospitals, clinics, and specialized medical facilities.

The company’s devices are authorised under EU regulations and are listed in the eudamed database. All products fall under Class IIa classification, requiring conformity assessment procedures as defined by the Medical Device Regulation (MDR). Technology S.R.L. 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 Technology S.R.L. manufacture?

Technology S.R.L. specializes in Class IIa medical devices primarily used in diagnostic imaging and radiation therapy. Their portfolio includes devices like X-ray imaging systems, mammography units, and fluoroscopy equipment, which are designed for clinical and procedural applications in hospitals, clinics, and specialized medical facilities.

Where is Technology S.R.L. based?

Technology S.R.L. is headquartered in Italy. The company’s location in Italy aligns with its focus on manufacturing and distributing medical devices that comply with European Union regulations.

Which regulatory registries list Technology S.R.L.’s devices?

Technology S.R.L.’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements for Class IIa devices.

How are Technology S.R.L.’s devices classified under EU regulations?

All of Technology S.R.L.’s devices fall under Class IIa classification under the Medical Device Regulation (MDR). This classification requires a conformity assessment process, including technical documentation review and involvement of a Notified Body, to ensure safety, performance, and compliance before market placement.

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

Information

Country
Italy
Address
7/B, VIA GARGANO, MILANO, Italy
Phone
+39 0257303118
PRRC contact
GABRIELLA ARMENIA
EUDAMED SRN
IT-MF-000035728