Broadland Rubber Industries Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Broadland Rubber Industries Sdn Bhd makes
Broadland Rubber Industries Sdn Bhd manufactures latex patient examination gloves designed for clinical use, providing barrier protection during medical procedures.
These products are classified as Class I devices under regulatory frameworks and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891636
510(k) 510(k)
Frequently asked questions
How many devices does Broadland Rubber Industries Sdn Bhd have in the registry?
The registry currently lists 1 device for Broadland Rubber Industries Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Broadland Rubber Industries Sdn Bhd's devices?
Among its 1 most recently registered device, Broadland Rubber Industries Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Broadland Rubber Industries Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Broadland Rubber Industries Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Broadland Rubber Industries Sdn Bhd in the registry?
The most recently registered devices listed for Broadland Rubber Industries Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).