Marketing Development Intl.
Country not established
- Devices
- 1
What Marketing Development Intl. makes
Marketing Development Intl. manufactures the MDI System II, a plethysmograph used for measuring changes in limb volume to assess conditions such as lymphedema or venous insufficiency.
The MDI System II is classified as a Class II device under FDA regulations and is listed in the 510(k) registry. The company is based in the United States.
Catalogue
Plethysmograph (Mdi System Ii) Ref K760504
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marketing Development Intl. have in the registry?
The registry currently lists 1 device for Marketing Development Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marketing Development Intl.'s devices?
Among its 1 most recently registered device, Marketing Development Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Marketing Development Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Marketing Development Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marketing Development Intl. in the registry?
The most recently registered devices listed for Marketing Development Intl. include PLETHYSMOGRAPH (MDI SYSTEM II).