Hospal
Country not established
- Devices
- 1
What Hospal makes
Hospal manufactures the Bioprime™ Kit, a medical device designed for use in vascular access procedures, including the preparation and priming of catheters to reduce infection risk during patient care.
The Bioprime™ Kit is classified as a Class II device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Bioprime Tm Kit Ref K892932
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hospal have in the registry?
The registry currently lists 1 device for Hospal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hospal's devices?
Among its 1 most recently registered device, Hospal has devices listed in FDA 510(k) (1 device).
What risk classes do Hospal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hospal's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hospal in the registry?
The most recently registered devices listed for Hospal include BIOPRIME TM KIT.