Max Staubli, Ltd.
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Max Staubli, Ltd. makes
Max Staubli, Ltd. manufactures catheter valves, including the KV 100 and KV 100EH models, designed for use in medical drainage applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Catheter Valves Kv 100 & Kv 100EH Ref K861699
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Max Staubli, Ltd. have in the registry?
The registry currently lists 1 device for Max Staubli, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Max Staubli, Ltd.'s devices?
Among its 1 most recently registered device, Max Staubli, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Max Staubli, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Max Staubli, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Max Staubli, Ltd. in the registry?
The most recently registered devices listed for Max Staubli, Ltd. include CATHETER VALVES KV 100 & KV 100EH.