Rindumas Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 1
What Rindumas Sdn Bhd makes
Rindumas Sdn Bhd manufactures latex patient examination gloves, designed for clinical use during medical procedures and examinations.
These gloves 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 (Latex) Ref K891502
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rindumas Sdn Bhd have in the registry?
The registry currently lists 1 device for Rindumas Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rindumas Sdn Bhd's devices?
Among its 1 most recently registered device, Rindumas Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Rindumas Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rindumas Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rindumas Sdn Bhd in the registry?
The most recently registered devices listed for Rindumas Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).