Mega Wijaya Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Mega Wijaya Sdn. Bhd. makes
Mega Wijaya Sdn. Bhd. manufactures latex patient examination gloves, designed for clinical use during medical procedures.
The company’s product portfolio is regulated under FDA’s Class I device classification and is listed in the 510(k) registry. The manufacturer is based in the United States.
Catalogue
Megatex Patient Examination Gloves (Latex) Ref K891852
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mega Wijaya Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Mega Wijaya Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mega Wijaya Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Mega Wijaya Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mega Wijaya Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mega Wijaya Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mega Wijaya Sdn. Bhd. in the registry?
The most recently registered devices listed for Mega Wijaya Sdn. Bhd. include MEGATEX PATIENT EXAMINATION GLOVES (LATEX).