Praesidia S.r.l.
Country not established
- Devices
- 1
What Praesidia S.r.l. makes
Praesidia S.R.L. manufactures the FLEXIGRIP STERNAL CLOSURE SYSTEM (models FG0200 through FG0400), a device designed for sternal wound closure following cardiac surgery.
The FLEXIGRIP STERNAL CLOSURE SYSTEM is classified as a Class II medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: CE MDR 510(k) Registry: EUDAMED510(k)
Frequently asked questions
How many devices does Praesidia S.R.L. have in the registry?
The registry currently lists 1 device for Praesidia S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Praesidia S.R.L.'s devices?
Among its 1 most recently registered device, Praesidia S.R.L. has devices listed in EUDAMED (1 device) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Praesidia S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Praesidia S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Praesidia S.R.L. in the registry?
The most recently registered devices listed for Praesidia S.R.L. include FLEXIGRIP STERNAL CLOSURE SYSTEM, MODEL FG0200 THROUGH FG0400 (NONE SIZES).