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Patient information

This website contains safety and performance information of products manufactured by Terumo Europe N.V. that are certified under the Medical Device Regulation (EU) 2017/745 (Annex I, chapter III, 23.1 general requirements)

Product type
Stents
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 Revision 1

Patient information - Ultimaster Nagomi™

In this document you will find all relevant information on your implant: Ultimaster Nagomi™ Sirolimus eluting coronary stent system

Information in the selected document may be available in multiple languages.

Document content may be subject to change.