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)
To consult the Patient Information Leaflets for Australia, please click here.
Revision 1
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.
This site uses cookies. Functional cookies are necessary for the use of this website and cannot be refused. Other cookies are only placed if you choose to do so. For further information please read our Privacy and cookies notice.
This site uses cookies. Functional cookies are necessary for the use of this ... website and cannot be refused. Other cookies are only placed if you choose to do so. For further information, please read our Privacy and cookies notice.
Essential cookies to ensure the website functions well.
Cookies to help us measure the general use of our website.
Cookies that save personal information while browsing.
