Sti Medical Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 2
What Sti Medical Sdn Bhd makes
Sti Medical Sdn Bhd makes patient latex examination gloves that are powdered and non-sterile, as well as patient examination gloves that are powder-free and non-sterile.
These devices are classified as Class I and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sti Medical Sdn Bhd have in the registry?
The registry currently lists 2 devices for Sti Medical Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sti Medical Sdn Bhd's devices?
Among its 2 most recently registered devices, Sti Medical Sdn Bhd has devices listed in FDA 510(k) (2 devices).
What risk classes do Sti Medical Sdn Bhd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sti Medical Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sti Medical Sdn Bhd in the registry?
The most recently registered devices listed for Sti Medical Sdn Bhd include PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) and PATIENT EXAMINATION GLOVES (POWDER FREE-NON STERILE).