Clinical Plastic Products SA
Country not established
- Devices
- 1
What Clinical Plastic Products SA makes
Clinical Plastic Products SA manufactures the JET PORT PLUS catheter system, a device designed for vascular access and infusion therapy.
The JET PORT PLUS catheter system is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Jet Port Plus Catheter System Ref K000125
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Plastic Products SA have in the registry?
The registry currently lists 1 device for Clinical Plastic Products SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Plastic Products SA's devices?
Among its 1 most recently registered device, Clinical Plastic Products SA has devices listed in FDA 510(k) (1 device).
What risk classes do Clinical Plastic Products SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Clinical Plastic Products SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Plastic Products SA in the registry?
The most recently registered devices listed for Clinical Plastic Products SA include JET PORT PLUS CATHETER SYSTEM.