Besglove Healthcare Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Besglove Healthcare Sdn. Bhd. makes
The company manufactures pre-powdered latex examination gloves designed for medical and clinical use, intended to provide barrier protection during examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Prepowdered Latex Examination Glove Ref K970313
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Besglove Healthcare Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Besglove Healthcare Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Besglove Healthcare Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Besglove Healthcare Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Besglove Healthcare Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Besglove Healthcare Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Besglove Healthcare Sdn. Bhd. in the registry?
The most recently registered devices listed for Besglove Healthcare Sdn. Bhd. include PREPOWDERED LATEX EXAMINATION GLOVE.