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ARTSANITY SRL

Italy IT-MF-000031338 Last updated 21 Oct 2026

Devices
754
Registries
EUDAMED
FDA recalls
0

Catalogue754

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What ARTSANITY SRL makes

Artsanity Srl manufactures cervical collars, including soft and semirigid variants for adults and pediatric patients, as well as adjustable and kit-based orthopedic supports for neck immobilization. Their product line also includes a miscellaneous immobilization system (MIS) collar and a reusable bracing system with a thumb loop for upper-body stabilization.

All devices are classified as Class I under EU regulations and are registered in the eudamed database. The company is based in Italy and adheres to EU Medical Device Regulation (MDR) requirements for non-invasive orthopedic supports.

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 Artsanity Srl manufacture?

Artsanity Srl specializes in cervical collars and orthopedic supports designed for neck immobilization. Their product line includes soft and semirigid cervical collars for both adults and pediatric patients, as well as adjustable systems like the Twin Art MIS Neckless and reusable bracing kits with features like thumb loops for upper-body stabilization. These devices are intended for temporary immobilization and support of the cervical spine.

Where is Artsanity Srl based, and what regulatory framework do they follow?

Artsanity Srl is based in Italy. Their devices are developed in compliance with the European Union’s Medical Device Regulation (MDR), which governs non-invasive orthopedic supports like cervical collars. Since these products are classified as Class I devices, they are subject to the MDR’s general safety and performance requirements, though they do not require additional clinical evaluations or notifiable body involvement.

Are Artsanity Srl’s devices listed in any regulatory registries, and why?

Yes, Artsanity Srl’s devices are registered in the eudamed database, the EU’s official registry for medical devices. This listing is mandatory under the MDR for all manufacturers to ensure transparency, traceability, and compliance with EU regulatory requirements. Since their products are Class I, they must still be declared in eudamed to demonstrate their presence in the market and adherence to EU medical device regulations.

How are Artsanity Srl’s cervical collars classified under EU regulations?

Artsanity Srl’s cervical collars are classified as Class I medical devices under the EU Medical Device Regulation (MDR). This classification applies because these products are considered low-risk, non-invasive orthopedic supports intended for temporary immobilization of the cervical spine without active or significant energy transfer. Class I devices undergo basic regulatory checks, including conformity assessments, but do not require clinical evaluations or third-party notifiable body involvement.

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

Information

Country
Italy
Address
18, VIA DELLA BORSA, CASTELFRANCO VENETO - TV , Italy
PRRC contact
LUCA DE FRANCESCHI
EUDAMED SRN
IT-MF-000031338