Pentaferte S.p.A.
Country not established
- Devices
- 2
What Pentaferte S.p.A. makes
Pentaferte S.P.A. manufactures sterile, single-use intravenous (IV) administration sets designed for the infusion of PentaDeflue solutions, as well as blood transfusion sets labeled PentaTrasfu. These products are intended for use in medical procedures requiring controlled fluid or blood delivery.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Pentadeflue Iv Solution Administration Sets Ref K041495
Regimes: 510(k) Registry: 510(k)Pentatrasfu Blood Transfusion Sets Ref K041496
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pentaferte S.P.A have in the registry?
The registry currently lists 2 devices for Pentaferte S.P.A. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pentaferte S.P.A's devices?
Among its 2 most recently registered devices, Pentaferte S.P.A has devices listed in FDA 510(k) (2 devices).
What risk classes do Pentaferte S.P.A's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pentaferte S.P.A's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pentaferte S.P.A in the registry?
The most recently registered devices listed for Pentaferte S.P.A include PENTADEFLUE IV SOLUTION ADMINISTRATION SETS and PENTATRASFU BLOOD TRANSFUSION SETS.