Parexel International
Country not established
- Devices
- 1
What Parexel International makes
The company manufactures arterial filters, including the D731 MICRO 27 PH.I.S.I.O. and D733 MICRO 40 PH.I.S.I.O. models, designed for vascular applications to prevent embolic debris during procedures.
These devices are classified as Class II under regulatory frameworks and are listed via 510(k) submissions with the FDA. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Parexel International have in the registry?
The registry currently lists 1 device for Parexel International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Parexel International's devices?
Among its 1 most recently registered device, Parexel International has devices listed in FDA 510(k) (1 device).
What risk classes do Parexel International's devices fall under?
Among its 1 most recently registered device, the classes recorded for Parexel International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Parexel International in the registry?
The most recently registered devices listed for Parexel International include D731 MICRO 27 PH.I.S.I.O. AND D733 MICRO 40 PH.I.S.O. ARTERIAL FILTERS.