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Imaginalis Srl

Italy IT-MF-000026523 Last updated 21 Oct 2026

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Devices
3
Registries
EUDAMED
FDA recalls
0

Catalogue3

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 1450769 1 Amended

    Quality management system EU MDR

    Issued
    10 Oct 2025
    Expires
    18 Jul 2029
    Reason
    Other

Related companies

Notified bodies

What Imaginalis Srl makes

Imaginalis Srl produces medical devices such as limb supports and imaging equipment like the See Factor CT3 and See Factor aBordo. These devices are designed to provide support and diagnostic capabilities in medical settings. The company's products cater to various needs, including patient care and medical imaging.

The company's portfolio is regulated under Class I and Class IIb device classes and is listed in the Eudamed registry. Imaginalis Srl is based in Italy. The regulatory oversight ensures that the devices meet specific safety and performance standards.

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 Imaginalis Srl produce?

Imaginalis Srl produces medical devices such as limb supports and imaging equipment, including the See Factor CT3 and See Factor aBordo, which are designed to provide physical support and diagnostic capabilities in medical settings for patient care and imaging needs.

Where is Imaginalis Srl based?

Imaginalis Srl is based in Italy, as indicated by the country code IT in the device data, which specifies the company's location for regulatory and operational purposes.

In which regulatory registry are Imaginalis Srl's devices listed?

Imaginalis Srl's devices are listed in the Eudamed registry, which is the European Union's medical device database used for tracking devices placed on the market in the EU.

How are Imaginalis Srl's devices classified under regulatory frameworks?

Imaginalis Srl's devices are regulated under Class I and Class IIb classifications, meaning they range from low-risk devices like limb supports to higher-risk devices such as certain imaging equipment requiring more stringent conformity assessment.

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

Information

Country
Italy
Address
13-15, Via Rodolfo Morandi, Sesto Fiorentino (FI), Italy
Phone
+39 055 0463727
PRRC contact
Simona Ciappi
EUDAMED SRN
IT-MF-000026523