Patiria Sdn.Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Patiria Sdn.Bhd. makes
Patiria Sdn.Bhd. manufactures latex patient examination gloves, designed for use during clinical procedures to maintain hygiene and reduce infection risk.
These products are classified as Class I medical devices under US regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892589
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Patiria Sdn.Bhd. have in the registry?
The registry currently lists 1 device for Patiria Sdn.Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Patiria Sdn.Bhd.'s devices?
Among its 1 most recently registered device, Patiria Sdn.Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Patiria Sdn.Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Patiria Sdn.Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Patiria Sdn.Bhd. in the registry?
The most recently registered devices listed for Patiria Sdn.Bhd. include PATIENT EXAMINATION GLOVES (LATEX).