Sepax kits are integral to our Sepax Cell Separation System. They are supplied sterile for single-use and enable a functionally-closed environment to separate cellular product into its components.
The CS-530.4b kit is designed for processing umbilical cord blood (UCB) in order to concentrate the nucleated cell fraction into a double-compartment CryoSC-Db cryobag.
|1||Separation Chamber||220 mL spinning chamber enabling the centrifugation and transfer of processed product|
|2||Line Pressure Monitor||0.2 µm filter that connects to the Sepax pressure sensor|
|3||Stopcock Manifold||Three automatically controlled rotational valves to direct fluid flow|
|4||Drip Chamber||200 μm filter to block blood clots and trap air bubbles|
|5||Initial Line||Connects the kit to the initial bag via a spike or SCD connection|
|6||Cryobag||CryoSC-Db cryobag with 25 mL storage capacity|
|7||By-product Bag||500 mL PVC by-product bag to collect plasma|
|8||DMSO Extension Line||A line equipped with leur port connections for adding cryoprotectant solution|
|9||DMSO Vial Spike||Needle with luer port for connecting cryoprotectant solution|
|10, 11||Final line||Final line with luer and sampling ports|
|Kit / protocol||UCB||UCB-HES|
Store kits in a clean and dry environment without chemical or biological contamination within the following conditions:
|Mode||In operation||Storage and transport|
|Temperature||+7 to +27°C||+4 to +40°C|
|Relative humidity||30 to 75%, non-condensing||20 to 75%, non-condensing|
Shelf life: Two years from the date of manufacture.
Sterilization: Ethylene oxide.
Material: Standard medical grade PVC, PP, EVA, and other materials.
Biocompatibility: ISO 10993-1
Fluid path: Non-pyrogenic
The CS-530.4b is CE marked and complies with the applicable requirements of the 93/42/EEC Medical Device Directive. Confirm with your local regulatory authority for compliance with other regulations.
|Product Division||Laboratory Division|