Scandimed. A.S.
Country not established
- Devices
- 2
What Scandimed. A.S. makes
Scandimed A.S. manufactures medical devices for gastrointestinal procedures, specifically the Auto-Band Ligator and the Varices Needle.
These products are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Auto-Band Ligator Ref K031236
Regimes: 510(k) Registry: 510(k)Varices Needle Ref K031238
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scandimed. A.S. have in the registry?
The registry currently lists 2 devices for Scandimed. A.S.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scandimed. A.S.'s devices?
Among its 2 most recently registered devices, Scandimed. A.S. has devices listed in FDA 510(k) (2 devices).
What risk classes do Scandimed. A.S.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Scandimed. A.S.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scandimed. A.S. in the registry?
The most recently registered devices listed for Scandimed. A.S. include AUTO-BAND LIGATOR and VARICES NEEDLE.