Medie Group
Country not established
- Devices
- 1
What Medie Group makes
Medie Group manufactures the Dr. Hesse’s Insect Poison Remover, a Class I device designed for the removal of insect venom or residue from skin.
The device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Dr. Hessel's Insect Poison Remover Ref K844048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medie Group have in the registry?
The registry currently lists 1 device for Medie Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medie Group's devices?
Among its 1 most recently registered device, Medie Group has devices listed in FDA 510(k) (1 device).
What risk classes do Medie Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medie Group's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medie Group in the registry?
The most recently registered devices listed for Medie Group include DR. HESSEL'S INSECT POISON REMOVER.