Where can I find the REF number or the UDI-DI of my product?
Before using any Sutter device - or performing reprocessing procedures - please consult the relevant Instructions for Use (IFU). These documents are regularly updated, and the most current version is always available on this platform.
To access the correct IFU, enter the article number (REF, found on the product label, see sample label) or the UID-ID (found on the product label, see sample label).
Please note: IFUs may only become available after a product has been transitioned to MDR compliance.
This website provides healthcare professionals with access to IFUs and related product information for Sutter Medizintechnik GmbH. It is intended solely for professional and business use.
By entering this site, you acknowledge that it is a private platform restricted to authorized users worldwide. Any unauthorized access, use, or modification is strictly prohibited and may result in civil or criminal penalties under applicable laws.
Usage of this site may be monitored and recorded for security and administrative purposes. If such monitoring reveals evidence of unlawful activity, Sutter reserves the right to share this information with law enforcement authorities.
By continuing, you confirm that you accept the Terms of Use, which can be accessed via the link in the bottom left corner of each page.
You will find the information regarding the processing of your personal data under our privacy policy.
© Sutter Medizintechnik GmbH. All rights reserved.
UnderstoodTo the homepage
The contact form is intended for use by medical professionals only.
The mandatory fields are required by law.