Selefar S.r.l.
Italy Last updated 17 Sep 2026
- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Hot Box 3C Ref Hot Box Technical data sheet
Pile-UpS Ref SE-PUS
Hot Box 2C Ref Hot Box Technical data sheet
Pile-UpSP Supporto su ruota a pensile Ref SE-PUSP
What Selefar S.r.l. makes
Selefar S.r.l. manufactures Class I medical devices primarily for laboratory and research use, including heated incubators (Hot Box 3C, Hot Box 2C) and specialized support systems for suspended samples (Pile-UpS, Pile-UpSP Supporto su ruota a pensile). These devices are designed for controlled environmental conditions and sample organization in scientific settings.
The company’s products are listed under the EU Medical Device Regulation (MDR) in the eudamed database as Class I devices. Selefar S.r.l. is based in Italy and adheres to EU regulatory requirements for these categories.
Frequently asked questions
How many devices does Selefar S.r.l. have in the registry?
The registry currently lists 4 devices for Selefar S.r.l.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Selefar S.r.l.'s devices?
Among its 4 most recently registered devices, Selefar S.r.l. has devices listed in EUDAMED (4 devices).
What risk classes do Selefar S.r.l.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Selefar S.r.l.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Selefar S.r.l. in the registry?
The most recently registered devices listed for Selefar S.r.l. include Hot Box 3C, Pile-UpS, Hot Box 2C and Pile-UpSP Supporto su ruota a pensile.
Information
- Address
- 3, Via del Caravaggio, Milano, Italy
- Website
- selefar.it
- [email protected]
- PRRC contact
- Roberto Fiorito
- EUDAMED SRN
- IT-MF-000031484