Scandimed International
Country not established
- Devices
- 2
What Scandimed International makes
Scandimed International makes auto-band ligators and modifications to auto-band ligators.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Modification To Auto-Band Ligator Ref K083556
Regimes: 510(k) Registry: 510(k)Auto-Band Ligator Ref K081142
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scandimed International have in the registry?
The registry currently lists 2 devices for Scandimed International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scandimed International's devices?
Among its 2 most recently registered devices, Scandimed International has devices listed in FDA 510(k) (2 devices).
What risk classes do Scandimed International's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Scandimed International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scandimed International in the registry?
The most recently registered devices listed for Scandimed International include MODIFICATION TO AUTO-BAND LIGATOR and AUTO-BAND LIGATOR.