Resources

Documents relating to the use of the INTERCEPT™ Blood System. Search for brochures, instructions for use, manuals, technical data sheets, and more.

The INTERCEPT™ Blood System is registered in Europe as a Class III medical device. The INTERCEPT platelet system received the CE Mark in 2002.
The INTERCEPT™ Blood System is registered in Europe as a Class III medical device. The INTERCEPT plasma system received the CE Mark in 2006.
The INTERCEPT™ Blood Systems for platelets and plasma are produced to the ISO 13485:2016 quality standard as certified by TÜV SÜD. At Cerus we are committed to continual improvement of our quality management system.
The INTERCEPT Illuminator is a Class I accessory to the INTERCEPT Blood System and is CE Marked according to Annex VII, EC Declaration of Conformity.