Pentaferte, S.r.l.
ItalyFDA applicant, unverified
- Devices
- 1
What Pentaferte, S.r.l. makes
Pentaferte, S.R.L. manufactures medical devices such as single-use syringes that come in various sizes. These syringes are examples of the products the company produces. The devices are used for medical purposes.
The company's portfolio, including devices like the Pentaferte single-use syringes, is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pentaferte, S.R.L. have in the registry?
The registry currently lists 1 device for Pentaferte, S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pentaferte, S.R.L.'s devices?
Among its 1 most recently registered device, Pentaferte, S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Pentaferte, S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pentaferte, S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pentaferte, S.R.L. in the registry?
The most recently registered devices listed for Pentaferte, S.R.L. include PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES.