Fiberweb North America, Inc.
Country not established
- Devices
- 1
What Fiberweb North America, Inc. makes
Fiberweb North America, Inc. manufactures STERISURE Sterilization Wrap, a barrier material designed for use in medical sterilization processes to protect packaged instruments and devices from contamination during autoclave or ethylene oxide sterilization.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Sterisure Sterilization Wrap Ref K944854
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fiberweb North America, Inc. have in the registry?
The registry currently lists 1 device for Fiberweb North America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fiberweb North America, Inc.'s devices?
Among its 1 most recently registered device, Fiberweb North America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fiberweb North America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fiberweb North America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fiberweb North America, Inc. in the registry?
The most recently registered devices listed for Fiberweb North America, Inc. include STERISURE STERILIZATION WRAP.