Asep-Pro, Inc.
Country not established
- Devices
- 1
What Asep-Pro, Inc. makes
Asep-Pro, Inc. manufactures self-sealing sterilization pouches designed to maintain sterility during medical procedures. These pouches are engineered to allow visibility of the contents while ensuring a secure, leak-proof barrier for packaged instruments and supplies.
The company’s sterilization pouches are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The products are intended for use in healthcare settings in the United States.
Catalogue
See-Thru Self Sealing Sterilization Pouch Ref K940807
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asep-Pro, Inc. have in the registry?
The registry currently lists 1 device for Asep-Pro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asep-Pro, Inc.'s devices?
Among its 1 most recently registered device, Asep-Pro, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Asep-Pro, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Asep-Pro, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Asep-Pro, Inc. in the registry?
The most recently registered devices listed for Asep-Pro, Inc. include SEE-THRU SELF SEALING STERILIZATION POUCH.