Pierrel SpA
Country not established
Pierrel SpA is a medical device manufacturer, with 1 device listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 1
Registry facts
- Registries
- FDA GUDID 1
- Device classes
- FDA Class II 1
- Identifiers
- DUNS 458463044
What Pierrel SpA makes
Pierrel SPA manufactures oral lesion examination lights, including the G.o.c.c.l.e.s. light, designed for visual inspection of oral tissues in clinical settings.
The company’s devices are classified as Class II under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Regimes: 510(k) Registry: GUDID
Company details
- DUNS number
- 458463044
- Phone
- +390823626111
Frequently asked questions
How many devices does PIERREL SPA have in the registry?
The registry currently lists 1 device for PIERREL SPA. Devices recorded under merged duplicate company entries are counted once.
Which registries list PIERREL SPA's devices?
Among its 1 most recently registered device, PIERREL SPA has devices listed in FDA GUDID (1 device).
What risk classes do PIERREL SPA's devices fall under?
Among its 1 most recently registered device, the classes recorded for PIERREL SPA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PIERREL SPA in the registry?
The most recently registered devices listed for PIERREL SPA include G.o.c.c.l.e.s. light.