Commfields (M) Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Commfields (M) Sdn. Bhd. makes
Commfields (M) Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
The company’s product portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892609
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Commfields (M) Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Commfields (M) Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Commfields (M) Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Commfields (M) Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Commfields (M) Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Commfields (M) Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Commfields (M) Sdn. Bhd. in the registry?
The most recently registered devices listed for Commfields (M) Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).