Pentaferte Italia S.r.l.
ItalyFDA applicant, unverified FDA FEI 3004756837
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Pentaferte Italia S.r.l. makes
Pentaferte Italia S.R.L. manufactures ENFit enteral syringes, including the NUTRIFIT line and ENFit Enteral Pump Syringes under the PENTA ENFit and NUTRIFIT brands.
The company's products are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
ENFit enteral syringes (NUTRIFIT) Ref K211661
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004756837
- Address
- Viale Piane Nocella, 23, CAMPLI Teramo
Frequently asked questions
How many devices does Pentaferte Italia S.R.L. have in the registry?
The registry currently lists 2 devices for Pentaferte Italia S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pentaferte Italia S.R.L.'s devices?
Among its 2 most recently registered devices, Pentaferte Italia S.R.L. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pentaferte Italia S.R.L.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pentaferte Italia S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pentaferte Italia S.R.L. in the registry?
The most recently registered devices listed for Pentaferte Italia S.R.L. include ENFit enteral syringes (NUTRIFIT) and ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT.