Sepax 2 S-100

The Sepax 2 S-100 is a mobile, closed capability system that efficiently processes umbilical cord blood, bone marrow, peripheral blood or other blood derivatives, as permitted by applicable regulatory requirements. The fundamental scientific technology relies on a separation chamber that provides both separation through rotation of the syringe chamber (centrifugation) and component transfer through displacement of the syringe piston. An optical sensor measures the light absorbency of the separated components and manages the flow direction of each of them in the correct output container.


  Sepax 2 features

External design


Lightweight housing, one-handed separation chamber pit closure system




W: 27 cm, L: 40 cm, H: 46 cm (10.6” x 15.7”, 18.1”),17 kg (37.5 lbs)


User interface


Color touchscreen display, intuitive graphical user interface (GUI)


Electronics and communication


Windows XP embedded, GMAP, USB, and Ethernet


Data saving capacity


32 logfiles, 50 patfiles, and 50 report files (PDF)


Core technology


Electric centrifugation motor, pneumatic piston drive circuitry


Optical line sensor


Red/blue transmitted LEDs
Red/blue scatters LEDs


Traceability function


Barcode reader with multiple code reading capabilities and desktop printer.
Full procedural data management with PDF report and procedural graph.

Unique Features

  • The user interface combines touch-screen technology and active procedural guidance to easily monitor procedural steps. An integrated help guide provides live assistance in case of problems.
  • Track procedural data with automatic printouts of procedure reports with all traceability IDs integrated, reflecting the importance of efficient and secured traceability of each processed unit.
  • Connect to local networks through an ethernet connection port in order to receive online support through secured remote access.
  • Several USB ports allowing communication with peripherals such as a barcode reader, a printer and a USB key used to store and transfer procedural files to a computer.

Regulatory Statement

The Sepax 2 S-100 is CE marked and complies with the directive 93/42/CEE for medical devices, including the electrical safety standard IEC 60601-1. Design control activities have been performed to ensure its safety and performance. Confirm with your local regulatory authority for compliance with other regulations.


Environmental Conditions

Only operate on a flat, stable, horizontal, and clean surface. Use it in an open environment to allow sufficient ventilation. Operate and store it within the following conditions:

Operation Storage and transport



+7 to +27°C


0 to +50°C


Relative humidity


30 to 75 %, non-condensing


20 to 75 %, non-condensing


Product Specifications

Description Parametres
Product Division Laboratory Division
Brand Cytiva

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Medical Division

Laboratory Division

Industry Business Unit