Epilog is part of Clouds of Care NV, which is the legal manufacturer of the Persyst ESI powered by Epilog medical device (UDI-DI 5430000733021), CE marked in Europe and FDA cleared. The clinical service in which the device is used, is offered to healthcare professionals by:
Persyst Development Corporation
420 Stevens Avenue Suite 210,
Solana Beach, CA 92075
support@persyst.com
www.persyst.com
Report interpretation guideline
A report interpretation guideline is provided in electronic form, with current version (effective 2023-04-04) available at:
https://persystesi-information.s3.amazonaws.com/Guideline_Report_Interpretation%2BPersystESI.pdf.
For more details on how to provide input data and download results, please refer to the user guide of the Persyst software.
Notes:
- A PDF viewer is needed to display the report interpretation guideline.
- A paper copy can be requested for free within 7 days via support@persyst.com.
- A translation of the report interpretation guideline can be requested for free via support@persyst.com.