Instructions For Use (IFU) and Patient Information - FAQ
Frequently Asked Questions
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).
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.
No. Instructions for Use approved for each country must be used.
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.
Click on the download image in your search results and the PDF file will display in your web browser. The file can be saved, searched, or printed using Adobe Reader functionality. A free PDF reader is available via Adobe Systems.
The recommended web browsers are:
- Chrome. Visit https://www.google.com/chrome/ to download.
- Mozilla Firefox. Visit https://www.mozilla.org/firefox/new/ to download.
- Edge. Visit https://www.microsoft.com/en-us/edge/download to download.
- Safari. Please visit https://support.apple.com/downloads/safari to download.
Instructions for Use and Patient Information may be revised from time to time, please refer to the Getinge IFU search page for the most current version at the time of the procedure.
Contact customer service or your local Getinge representative or please contact us with a direct request for a paper copy.