F.P. Rubinstein Y Cia S.r.l.
Country not established
- Devices
- 1
What F.P. Rubinstein Y Cia S.r.l. makes
F.P. Rubinstein Y Cia S.R.L. manufactures the STARLIGHT (Model PD9012), a medical device designed for specific diagnostic or therapeutic applications in ophthalmology, likely related to retinal imaging or treatment.
The STARLIGHT (Model PD9012) is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Starlight, Model PD9012 Ref K073317
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does F.P. Rubinstein Y Cia S.R.L. have in the registry?
The registry currently lists 1 device for F.P. Rubinstein Y Cia S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list F.P. Rubinstein Y Cia S.R.L.'s devices?
Among its 1 most recently registered device, F.P. Rubinstein Y Cia S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do F.P. Rubinstein Y Cia S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for F.P. Rubinstein Y Cia S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from F.P. Rubinstein Y Cia S.R.L. in the registry?
The most recently registered devices listed for F.P. Rubinstein Y Cia S.R.L. include STARLIGHT, MODEL PD9012.