Prior to use, refer to the “Instructions for Use” for complete and specific indications, contraindications, all warnings, precautions and potential adverse events.
The pRELAX Vasospasm Treatment Device has received the CE Mark (CE 0297). This product is manufactured by femtos GmbH - Universitätsstraße 136 D-44799 Bochum Germany: https://femtos.de/ and distributed by phenox GmbH. It is not approved for sale nor is it available for sale or use in the United States. Products and associated components are not available in all countries or regions. Please contact your phenox representative for details regarding product availability.