The country may not have the regulatory requirements to approve online Instructions for Use at this time. The Instructions for Use will be provided with the product as a paper copy. If you require a copy of the Instructions for Use, please contact us with a direct request for a paper copy.

Catalogue/Reference number is identified by the symbol and can be found on the product labels, the patient implant card and/or on the device itself (when applicable).

No. Instructions for Use or Patient Information may be different based on the requirements of a country. You should only use the Instructions for Use or Patient Information specific to your country.