ARTSANITY SRL
Italy IT-MF-000031338 Last updated 21 Oct 2026
- Devices
- 886
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Guanto Di Contenzione Ref 0311
Fly Splint Gomito Ref FSE15
Collare Cerviale Rigido Ref 2062
Fly Splint Ginocchio Destro Ref FSK37 R
Fly Splint Avambraccio E Mano Destra Ref FSH71
Fly Splint Polso Ambidestro Ref FSW62
FLY SPLINT GINOCCHIO E PIEDE Destro Ref FSKF46 R
Fly Splint Ginocchio Destro Ref FSK34 R
Fly Splint Caviglia Mis S Ref FSA20
FLY SPLINT GINOCCHIO E PIEDE Sinistro Ref FSKF44 L
Collare Cervicale In Rotolo Ref 7010 8
FLY SPLINT GINOCCHIO Ambidestro Ref FSK34
Collare Cervicale In Rotolo Ref 7010 11
FLY SPLINT GINOCCHIO E PIEDE Sinistro Ref FSKF45 L
FLY SPLINT GINOCCHIO E PIEDE Sinistro Ref FSKF46 L
Fly Splint Caviglia In Equino Ref FSEQ8
FLY SPLINT GINOCCHIO E PIEDE Sinistro Ref FSKF47 L
Fly Splint Polso Ambidestro Ref FSW61
Collare Cervicale Rigido Ref 206PED
FLY SPLINT GOMITO Pediatrico Ref FSE14
COLLARE CERVICALE IN ROTOLO da 4 MT Ref 7070 10
Guanto Di Contenzione Ref 0312
Fly Splint Gomito Ref FSE17
FLY SPLINT GINOCCHIO E PIEDE Destro Ref FSKF45 R
Fly Splint Ginocchio E Piede Ambidestro Ref FSKF47
Collare Cervicale Philadelphia Ref 100/102
Collare Cervicale PHILADELPHIA Misura XS Ref 100/100
Fly Splint Avambraccio E Mano Sinistra Ref FSH74
Fly Splint Ginocchio Sinistro Ref FSK36 L
Fly Splint Ginocchio Destro Ref FSK35 R
Fly Splint Avambraccio E Mano Sinistra Ref FSH75
FLY SPLINT GINOCCHIO Ambidestro Ref FSK36
Guanto Di Contenzione Ref 0313
Fly Splint Avambraccio E Mano Destra Ref FSH72
Showing 851-886 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