Cytiva - Other Supplies - Life Science - Lab supplies

Liquid preparation and management
Easy to connect single-use components for robust mixing, easy handling, and convenient storage of bioprocess liquids.

Catalog No.		Product	Net Price
	CYT12410208	ReadyCircuit 200 L 3-D bag, with 4 ports having 20	742.5	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT12410207	ReadyCircuit 100 L 3-D bag, with 5 ports having 19	808.5	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT12410209	ReadyCircuit 200 L 3-D bag, with 5 ports having 21	843	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064847	ReadyCircuit 50 L 3-D bag, with 3 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064848	ReadyCircuit 100 L 3-D bag, with 3 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064849	ReadyCircuit 200 L 3-D bag, with 3 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064850	ReadyCircuit 500 L 3-D bag, with 3 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064854	ReadyCircuit 50 L Hiflow 3-D bag, with 4 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064855	ReadyCircuit 100 L Hiflow 3-D bag, with 4 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)
	CYT29064856	ReadyCircuit 200 L Hiflow 3-D bag, with 4 ports terminating in ReadyMates	Special offer	Add to Cart
For use with ReadyKart Connections ReadyMate disposable aseptic connectors Application Aseptic clarification and purification of vaccines and monoclonals.\nAntibodies, recombinant proteins, and plasmids.\nAseptic cell processing.\nEnvironments where terminal sterilization is not feasible.\nPreclinical through Phase II clinical trials.\nAreas where the risk of cross contamination is high Fast Trak drug development processes.\nSmall to midsize CMOs, biotech, and biopharmas seeking lean solutions or having concerns about crosscontamination in preclinical, Phase I and Phase II trials. Certificate of Analysis Yes Sterility Each component is sterile for all fluid-contact surfaces (per AAMI TIR 33:2005 and the principles of ISO/AAMI/ASTM 11137-1:2006) Animal Free Compliance Animal-free origin for wetted parts per EMEA/410/01 (alternatively-manufacturing under denaturing conditions). Endotoxin For process fluid contact surfaces, endotoxin level is < 0.25 EU/mL using water extraction method. Hemolysis Testing Hemolysis, ISO 10993-4 Material Compliance USP Biological Safety, Class VI for wetted parts, USP ⁸⁸ plastics requirements and FDA 21CFR177.1520 Tubing i.d. 19 mm (0.75 in)

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