Trans-Pacific Healthcare-USA
Country not established
- Devices
- 1
What Trans-Pacific Healthcare-USA makes
Trans-Pacific Healthcare-USA manufactures DRIPTROL, a medical device designed for intravenous fluid administration, ensuring precise dosing and infusion control in clinical settings.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Driptrol Ref K902808
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trans-Pacific Healthcare-USA have in the registry?
The registry currently lists 1 device for Trans-Pacific Healthcare-USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trans-Pacific Healthcare-USA's devices?
Among its 1 most recently registered device, Trans-Pacific Healthcare-USA has devices listed in FDA 510(k) (1 device).
What risk classes do Trans-Pacific Healthcare-USA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Trans-Pacific Healthcare-USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trans-Pacific Healthcare-USA in the registry?
The most recently registered devices listed for Trans-Pacific Healthcare-USA include DRIPTROL.