Global Medical Ent., Inc.
Country not established
- Devices
- 1
What Global Medical Ent., Inc. makes
Global Medical Ent., Inc. manufactures the PULMOMIST, a device designed for pulmonary drug delivery, likely targeting inhalation therapies for respiratory conditions.
The PULMOMIST is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pulmomist Ref K952326
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Global Medical Ent., Inc. have in the registry?
The registry currently lists 1 device for Global Medical Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Global Medical Ent., Inc.'s devices?
Among its 1 most recently registered device, Global Medical Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Global Medical Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Global Medical Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Global Medical Ent., Inc. in the registry?
The most recently registered devices listed for Global Medical Ent., Inc. include PULMOMIST.