Usci Ireland
Country not established
- Devices
- 2
What Usci Ireland makes
Usci Ireland manufactures percutaneous transluminal angioplasty (PTA) balloon dilatation catheters, including sizes 0.035 inches and standard 0.035-inch variants, designed for vascular dilation procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Optimus 0.035 Pta Balloon Dilatation Catheter Ref K082646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Usci Ireland have in the registry?
The registry currently lists 2 devices for Usci Ireland. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usci Ireland's devices?
Among its 2 most recently registered devices, Usci Ireland has devices listed in FDA 510(k) (2 devices).
What risk classes do Usci Ireland's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Usci Ireland's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usci Ireland in the registry?
The most recently registered devices listed for Usci Ireland include OPTIMUS 0.035 INCH PTA BALLOON DILATATION CATHETER and OPTIMUS 0.035 PTA BALLOON DILATATION CATHETER.