Medilatex Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Medilatex Sdn. Bhd. makes
Medilatex Sdn. Bhd. makes the CLIMAX device.
The CLIMAX device is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Climax Ref K991049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medilatex Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Medilatex Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medilatex Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Medilatex Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medilatex Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medilatex Sdn. Bhd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medilatex Sdn. Bhd. in the registry?
The most recently registered devices listed for Medilatex Sdn. Bhd. include CLIMAX.