Wagania Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Wagania Sdn. Bhd. makes
Wagania Sdn. Bhd. manufactures latex patient examination gloves designed for medical use, providing a barrier for healthcare professionals during clinical examinations.
The company’s product portfolio is classified under Class I devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Patient Examination Glove (Latex) Ref K892272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wagania Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Wagania Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wagania Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Wagania Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wagania Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wagania Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wagania Sdn. Bhd. in the registry?
The most recently registered devices listed for Wagania Sdn. Bhd. include PATIENT EXAMINATION GLOVE (LATEX).