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Cordis Europa, N.V.

Country not established

Devices
7

What Cordis Europa, N.V. makes

Cordis Europa manufactures percutaneous transluminal angioplasty (PTA) balloon dilatation catheters, including single-use and multi-stage dilators for vascular access, as well as transhepatic biliary stents delivered via .018-inch compatible systems. Products include wire-guided balloon dilators and high-pressure PTA balloons designed for coronary and peripheral interventions.

The company’s portfolio consists of Class II medical devices, primarily authorised via FDA 510(k) clearance. These products are listed under the FDA’s regulatory framework and are intended for use in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Cordis Europa, N.V. have in the registry?

The registry currently lists 7 devices for Cordis Europa, N.V.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cordis Europa, N.V.'s devices?

Among its 7 most recently registered devices, Cordis Europa, N.V. has devices listed in FDA 510(k) (7 devices).

What risk classes do Cordis Europa, N.V.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Cordis Europa, N.V.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cordis Europa, N.V. in the registry?

The most recently registered devices listed for Cordis Europa, N.V. include CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM, CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER, CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA and CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.