Perindustrian Masmuar Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 1
What Perindustrian Masmuar Sdn Bhd makes
Perindustrian Masmuar Sdn Bhd manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These gloves 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 K891830
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perindustrian Masmuar Sdn Bhd have in the registry?
The registry currently lists 1 device for Perindustrian Masmuar Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perindustrian Masmuar Sdn Bhd's devices?
Among its 1 most recently registered device, Perindustrian Masmuar Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Perindustrian Masmuar Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Perindustrian Masmuar Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Perindustrian Masmuar Sdn Bhd in the registry?
The most recently registered devices listed for Perindustrian Masmuar Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).