ARTSANITY SRL
Italy IT-MF-000031338 Last updated 21 Oct 2026
- Devices
- 886
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Palmare In Legno Ambidestro Imbottito Pediatrico M Ref 2502PED I
Ginocchiera 3P H. Cm. 40 Ref 2210
Ginocchiera H. Cm. 50 Mis. M Colore Nero Ref 2202 M N
Ginocchiera Knee-Mould H. Cm. 55 Mis. M Ref 7203 M
Clavisystem Deluxe Ref 3203
Corpetto Artfix Ref 45101
Cuscino Imbottito Nevada Mis. M Ref NEVADA M
Polsiera Modello Superior Mis. L Sx Ref SUPERIOR LSX
Polsiera Modello Superior Mis. Pediatrica Sx Ref SUPERIOR PSX
Arty-Gilet Ref 44102
Splint Per Dita Preformati Mis. 2 - Conf. 5 Pz Ref ARTIX 2/5
ROLL SPLINT 90x11 Ref 50026 GG
Palmare In Legno Ambidestro Imbottito Xs Ref 2501 I
Polsiera Modello Superior Mis. Xs Dx Ref SUPERIOR XSDX
Gomitiera In Cartone Mis. S Pediatrica Ref 2401PED
Ginocchiera 3P Knee-Mould H. Cm. 50 Ref 7211
Polsiera Modello Superior Mis. S Dx Ref SUPERIOR SDX
Ginocchiera H. Cm. 60 Mis. M Ref 2204 M
Palmare In Legno Ambidestro Imbottito Xl Ref 2505 I
Splint Per Dita Preformati Mis. 1 - Conf. 5 Pz Ref ARTIX 1/5
Palmare In Cartone Sagomato Destro Mis. M Ref 2512 DX
Cuscino Imbottito Nevada Mis. Xs Ref NEVADA XS
Splint Per Dita Preformati Mis. 5 Ref ARTIX 5
Cuscino Imbottito Nevada Mis. L Ref NEVADA L
Union Splint Scafoide Sinistro L/Xl Ref 900MI3 L
Splint Per Dita Preformati Mis. 5 - Conf. 1 Pz Ref ARTIX 5/1
Polsiera Modello Superior Mis. S Sx Ref SUPERIOR SSX
Palmare In Cartone Sagomato Sinistro Mis. S Ref 2511 SX
Splint Per Dita Preformati Mis. 7 - Conf. 1 Pz Ref ARTIX 7/1
Cuscino Imbottito Nevada Neonatale Ref NEVADA N
Showing 651-700 of 886
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.
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.
Information
- Country
- Italy
- Address
- 18, VIA DELLA BORSA, CASTELFRANCO VENETO - TV , Italy
- Website
- www.artsanity.it
- [email protected]
- PRRC contact
- LUCA DE FRANCESCHI
- EUDAMED SRN
- IT-MF-000031338