Medical Innovation Development
FranceFDA applicant, unverified
- Devices
- 1
What Medical Innovation Development makes
Medical Innovation Development manufactures the MIDSLEEVE, a sleeve device designed for use in medical procedures requiring secure attachment to limbs or extremities.
The MIDSLEEVE is classified as a Class II medical device under FDA regulations and is listed in the 510(k) registry. The company is based in the United States.
Catalogue
Midsleeve Ref K142548
Regimes: CE MDD 510(k) Registry: EUDAMED510(k)
Frequently asked questions
How many devices does Medical Innovation Development have in the registry?
The registry currently lists 1 device for Medical Innovation Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Innovation Development's devices?
Among its 1 most recently registered device, Medical Innovation Development has devices listed in EUDAMED (1 device) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Medical Innovation Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Innovation Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Innovation Development in the registry?
The most recently registered devices listed for Medical Innovation Development include MIDSLEEVE.