D.I.R.R.A. S.R.L.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What D.I.R.R.A. S.R.L. makes
D.I.R.R.A. S.R.L. manufactures surgical drape kits designed for use in sterile procedures to maintain contamination control during medical operations.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Surgical Drape Kit - D.I.R.R.A. SRL Ref K041080
510(k) 510(k)
Frequently asked questions
How many devices does D.I.R.R.A. S.R.L. have in the registry?
The registry currently lists 1 device for D.I.R.R.A. S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.I.R.R.A. S.R.L.'s devices?
Among its 1 most recently registered device, D.I.R.R.A. S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do D.I.R.R.A. S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D.I.R.R.A. S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D.I.R.R.A. S.R.L. in the registry?
The most recently registered devices listed for D.I.R.R.A. S.R.L. include SURGICAL DRAPE KIT - D.I.R.R.A. SRL.