Jamuri Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Jamuri Sdn. Bhd. makes
Jamuri Sdn. Bhd. manufactures patient examination gloves, designed for single-use medical procedures requiring sterile or clean hand protection.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K892779
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jamuri Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Jamuri Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jamuri Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Jamuri Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jamuri Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jamuri Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jamuri Sdn. Bhd. in the registry?
The most recently registered devices listed for Jamuri Sdn. Bhd. include PATIENT EXAMINATION GLOVES.