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 comprised of the INTERCEPT Processing Set for plasma ( a Class III medical device) and the INTERCEPT Illuminator (a Class IIa medical device). The INTERCEPT Processing Set for plasma received the CE Mark in 2006.
The INTERCEPT Blood System is comprised of the INTERCEPT Processing Set for platelets ( a Class III medical device) and the INTERCEPT Illuminator (a Class IIa medical device). The INTERCEPT Processing Set for platelets received the CE Mark in 2002.
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™ 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™ 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 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 in accordance with the quality standards of 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™ Blood System is registered in Europe as a Class III medical device. The INTERCEPT plasma system received the CE Mark in 2006.