Johor Bahru Emulsion Industries Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Johor Bahru Emulsion Industries Sdn. Bhd. makes
The company manufactures latex patient examination gloves, designed for single-use medical procedures to maintain sterility and reduce cross-contamination during clinical examinations.
These gloves are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891867
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johor Bahru Emulsion Industries Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Johor Bahru Emulsion Industries Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johor Bahru Emulsion Industries Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Johor Bahru Emulsion Industries Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Johor Bahru Emulsion Industries Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Johor Bahru Emulsion Industries Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Johor Bahru Emulsion Industries Sdn. Bhd. in the registry?
The most recently registered devices listed for Johor Bahru Emulsion Industries Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).