Pt. Trihasta Loka Persada
IndonesiaFDA applicant, unverified
- Devices
- 1
What Pt. Trihasta Loka Persada makes
Pt. Trihasta Loka Persada manufactures revised patient examination gloves, designed for clinical use in medical 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
Revised Patient Examination Gloves Ref K896411
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pt. Trihasta Loka Persada have in the registry?
The registry currently lists 1 device for Pt. Trihasta Loka Persada. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pt. Trihasta Loka Persada's devices?
Among its 1 most recently registered device, Pt. Trihasta Loka Persada has devices listed in FDA 510(k) (1 device).
What risk classes do Pt. Trihasta Loka Persada's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pt. Trihasta Loka Persada's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pt. Trihasta Loka Persada in the registry?
The most recently registered devices listed for Pt. Trihasta Loka Persada include REVISED PATIENT EXAMINATION GLOVES.