Sarmed SRL
ItalyFDA applicant, unverified FDA FEI 3005695808
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005695808
- Address
- via Centauro 24, IGLESIAS Sardegna
Frequently asked questions
How many devices does Sarmed Srl have in the registry?
The registry currently lists 1 device for Sarmed Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sarmed Srl's devices?
Among its 1 most recently registered device, Sarmed Srl has devices listed in FDA 510(k) (1 device).
What risk classes do Sarmed Srl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sarmed Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sarmed Srl in the registry?
The most recently registered devices listed for Sarmed Srl include SINGLE USE ESOPHAGEAL MANOMETEY CATHETERS AND SINGLE USE ANO-RECTAL MANOMETRY CATHETERS.