Phillippine Radiant C/O U.S. Polymer Industries
Country not established
- Devices
- 1
What Phillippine Radiant C/O U.S. Polymer Industries makes
The company manufactures Dunford Surgeon’s Sterile Gloves, a single-use, sterile barrier device designed for surgical and medical procedures to reduce contamination risk during procedures.
These gloves are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dunford Surgeon's Sterile Gloves Ref K880480
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phillippine Radiant C/O U.S. Polymer Industries have in the registry?
The registry currently lists 1 device for Phillippine Radiant C/O U.S. Polymer Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phillippine Radiant C/O U.S. Polymer Industries's devices?
Among its 1 most recently registered device, Phillippine Radiant C/O U.S. Polymer Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Phillippine Radiant C/O U.S. Polymer Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Phillippine Radiant C/O U.S. Polymer Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phillippine Radiant C/O U.S. Polymer Industries in the registry?
The most recently registered devices listed for Phillippine Radiant C/O U.S. Polymer Industries include DUNFORD SURGEON'S STERILE GLOVES.