Creative Plastic Technology
Country not established
- Devices
- 1
What Creative Plastic Technology makes
Creative Plastic Technology manufactures the MASTERSITE Needleless Luer Activated IV Connector (Model MS 1000), a sterile, single-use connector designed for intravenous fluid administration to reduce contamination risk during transfers.
The device is classified as Class II under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Creative Plastic Technology have in the registry?
The registry currently lists 1 device for Creative Plastic Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creative Plastic Technology's devices?
Among its 1 most recently registered device, Creative Plastic Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Creative Plastic Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Creative Plastic Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creative Plastic Technology in the registry?
The most recently registered devices listed for Creative Plastic Technology include MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000.