Mediserve International, Inc.
Country not established
- Devices
- 1
What Mediserve International, Inc. makes
Mediserve International, Inc. manufactures the GONODECTEN, a medical device designed for diagnostic or monitoring purposes in a specialized clinical context.
The GONODECTEN is classified as a Class I device under FDA regulations and is listed under the Premarket Approval (PMA) pathway. The company is based in the United States.
Catalogue
Gonodecten Ref P770010
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Mediserve International, Inc. have in the registry?
The registry currently lists 1 device for Mediserve International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediserve International, Inc.'s devices?
Among its 1 most recently registered device, Mediserve International, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Mediserve International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediserve International, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mediserve International, Inc. in the registry?
The most recently registered devices listed for Mediserve International, Inc. include GONODECTEN.