Medimex, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Medimex, Inc. makes
Medimex, Inc. manufactures continuous ventilators, including the ARF-1500, MVP-1500, and KMA-1300F models, designed for respiratory support in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Arf-1500 Continuous Ventilator Ref K860798
Regimes: 510(k) Registry: 510(k)Mvp-1500 Continuous Ventilator Ref K871009
Regimes: 510(k) Registry: 510(k)Kma-1300F Ref K841370
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medimex, Inc. have in the registry?
The registry currently lists 3 devices for Medimex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medimex, Inc.'s devices?
Among its 3 most recently registered devices, Medimex, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Medimex, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medimex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medimex, Inc. in the registry?
The most recently registered devices listed for Medimex, Inc. include ARF-1500 CONTINUOUS VENTILATOR, MVP-1500 CONTINUOUS VENTILATOR and KMA-1300F.