Dextran Products, Ltd.
Country not established
- Devices
- 1
What Dextran Products, Ltd. makes
Dextran Products, Ltd. manufactures CLEX, a Class I medical device designed for specific clinical applications involving dextran-based solutions.
The company’s portfolio is regulated under FDA 510(k) clearance and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
Clex Ref K833463
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dextran Products, Ltd. have in the registry?
The registry currently lists 1 device for Dextran Products, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dextran Products, Ltd.'s devices?
Among its 1 most recently registered device, Dextran Products, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dextran Products, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dextran Products, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dextran Products, Ltd. in the registry?
The most recently registered devices listed for Dextran Products, Ltd. include CLEX.