Ejs Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Ejs Sdn. Bhd. makes
Ejs Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892267
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ejs Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Ejs Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ejs Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Ejs Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ejs Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ejs Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ejs Sdn. Bhd. in the registry?
The most recently registered devices listed for Ejs Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).