Waterwide Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Waterwide Sdn. Bhd. makes
Waterwide Sdn. Bhd. manufactures latex patient examination gloves.
Their products are Class I devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Latex Patient Examination Gloves Ref K895194
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Waterwide Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Waterwide Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Waterwide Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Waterwide Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Waterwide Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Waterwide Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Waterwide Sdn. Bhd. in the registry?
The most recently registered devices listed for Waterwide Sdn. Bhd. include LATEX PATIENT EXAMINATION GLOVES.