Seac S.r.l.
Country not established
- Devices
- 1
What Seac S.r.l. makes
Seac S.R.L. manufactures the BRIO Automatic Sampling Unit, a device designed for automated sample collection and processing in laboratory settings.
The BRIO Automatic Sampling Unit is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Brio Automatic Samplinc Unit Ref K961209
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seac S.R.L. have in the registry?
The registry currently lists 1 device for Seac S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seac S.R.L.'s devices?
Among its 1 most recently registered device, Seac S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Seac S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Seac S.R.L.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seac S.R.L. in the registry?
The most recently registered devices listed for Seac S.R.L. include BRIO AUTOMATIC SAMPLINC UNIT.