Armak Tape Division
Country not established
- Devices
- 1
What Armak Tape Division makes
Armak Tape Division manufactures autoclave tape, a single-use barrier material designed to seal medical equipment and instruments during sterilization cycles in healthcare settings.
The autoclave tape portfolio is regulated as Class II devices under FDA 510(k) clearance requirements and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Ac-22 Autoclave Tape Ref K831722
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Armak Tape Division have in the registry?
The registry currently lists 1 device for Armak Tape Division. Devices recorded under merged duplicate company entries are counted once.
Which registries list Armak Tape Division's devices?
Among its 1 most recently registered device, Armak Tape Division has devices listed in FDA 510(k) (1 device).
What risk classes do Armak Tape Division's devices fall under?
Among its 1 most recently registered device, the classes recorded for Armak Tape Division's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Armak Tape Division in the registry?
The most recently registered devices listed for Armak Tape Division include AC-22 AUTOCLAVE TAPE.