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Cytiva (Cytiva China)

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BrandCytiva
OriginSweden
ModelWAVE 20/50
Maximum Working Volume25 L
Tray Sizes5 L / 10 L / 25 L
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BrandCytiva
OriginSweden
ModelÄKTA readyflux
TypeSingle-Use Tangential Flow Filtration (TFF) System
Application ScopeLab-Scale to Pilot-Scale Bioprocessing
Control SoftwareUNICORN 7.x or later
CompatibilityDeltaV™ DCS, ReadyToProcess Hollow-Fiber Cartridges, Xcellerex XDUO Single-Use Mixers, Third-Party Bag Mixers
Regulatory AlignmentDesigned for GLP/GMP environments
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BrandCytiva
OriginUSA
Manufacturer TypeAuthorized Distributor
Product CategoryImported
ModelXcellerex™ X-50
PricingUpon Request
Application DomainBiopharmaceutical Cell Culture
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BrandCytiva
OriginSweden
ModelUniFlux Tangential Flow Filtration System
Flow Rate Options10, 60, 120 L/min (400 L/min available on custom basis)
Vessel Capacity Range5–600 L (stainless steel or single-use mixing systems supported)
Automation PlatformUNICORN Software (21 CFR Part 11 compliant)
Application ScopeMicrofiltration (e.g., cell harvest) and Ultrafiltration (e.g., protein concentration & diafiltration)
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BrandCytiva
OriginUSA
ModelReadyToProcess WAVE 25
Maximum Working Volume25 L
Drive MechanismMotorized Rocking Platform with Adjustable Speed, Angle, and Motion Profile
Temperature ControlIntegrated Heated Tray with Dual Independent PID Loops (Dual-Mode Operation)
Weight MeasurementBuilt-in Load Cells with Auto-Calibration Capability
Gas TransferPassive O₂/CO₂ Exchange via Sterile Vent Filters (Heated Exhaust Filter Included)
Data StorageDual Mirrored SSDs + UNICORN Database Integration
Communication ProtocolOPC UA Compliant
ComplianceDesigned for GMP Environment
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BrandCytiva
OriginSwitzerland
ModelNanoAssemblr™ Spark™ Instrument
Sample Volume Range25–250 µL
Mixing TechnologyNxGen™ Microfluidic Vortex Mixing
Sterility DesignBSC-Compatible, Aseptic Operation Ready
Chip TypeSingle-Use, Gamma-Irradiated Cartridge
Scalability PathwaySeamless Transition to NanoAssemblr™ Ignite™ and NxGen™ Production Platforms
Regulatory ContextDesigned for GLP-compliant early-stage development, supports 21 CFR Part 11–ready software integration (optional)
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BrandCytiva
OriginSweden
ModelWave Cellbag
Sterilization MethodGamma Irradiation
Material ComplianceUSP Class VI
Regulatory DocumentationFDA-registered DMF on file
Intended UseResearch, Process Development, cGMP Manufacturing, Cell Therapy Production
Bag ConfigurationSingle-use, pre-sterilized, disposable bioprocess bag
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BrandCytiva
OriginSwitzerland
ModeliCELLis™ Nano Bioreactor System
Temperature RangeDouble-jacketed with TCU – 20–40 °C
Surface Area Range (iCELLis™ 500+)60–500 m²
Surface Area Range (iCELLis™ Nano)0.53–4 m²
ConfigurationSingle-use, integrated fixed-bed bioreactor
Operating ModesBatch and perfusion
ComplianceDesigned to support GMP-compliant manufacturing
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BrandCytiva
OriginSwitzerland
ModelNanoAssemblr™ Blaze™ System
Volume Range1 L (Blaze™) / up to 10 L (Blaze+™)
System ArchitectureClosed, single-use, GMP-ready process development platform
Core TechnologyNxGen™ microfluidic mixing
Regulatory AlignmentSupports FDA 21 CFR Part 11–compliant data integrity, GLP/GMP process transfer readiness
Disposable ComponentsNxGen™ single-use chips (with/without inline dilution), sterile tubing kits for external vessel integration
Downstream CompatibilityIntegrated TFF, sterile filtration, and fill-finish workflow support
Scalability PathwayDirect CPP/CQA transfer from Blaze™ → Blaze+™ → NanoAssemblr™ Production System
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BrandCytiva
OriginSwitzerland
Manufacturer TypeAuthorized Distributor
Product CategoryImported
ModelNanoAssemblr™ Commercial Manufacturing System
PricingUpon Request
Flow Rate Range6–48 L/h (dependent on disposable flow path kit)
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BrandCytiva
OriginImported
Manufacturer TypeAuthorized Distributor
Membrane Area Compatibility0.1–2.5 m² (cassette & hollow-fiber modules)
Predefined Process ProgramsUF Production, Normalized Water Permeability (NWP), Clean-in-Place (CIP), Water Rinse, Alkaline Hold
Regulatory AlignmentDesigned to support GMP, FDA 21 CFR Part 11, and EU Annex 11 compliance requirements
Software ArchitectureEmbedded control with audit trail, user access levels, and electronic signature capability
System FlexibilityModular configuration for lab-scale development, pilot-scale process validation, and small-batch cGMP manufacturing
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BrandCytiva
OriginSwitzerland
ModelNanoAssemblr™ GMP System
Flow Rate Range60–200 mL/min (3.6–12 L/h)
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BrandCytiva
OriginSweden
ModelÄKTA flux 6
ConfigurationSemi-automated TFF platform
Application ScopeConcentration, diafiltration, cell harvest & clarification
Membrane CompatibilityHollow-fiber modules & cassette-type membrane packs
Operating Volume Range50 mL – 6 L
Control InterfaceIntegrated touchscreen with real-time parameter monitoring
Data LoggingOnboard process recording (time-stamped, user-ID traceable)
Regulatory SupportCompliant with FDA 21 CFR Part 11 audit trail requirements for GMP-relevant workflows
Service FrameworkOptiRun lifecycle support program
Change NotificationWeb-based Change Control Notification (CCN) service
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BrandCytiva
OriginSwitzerland
Manufacturer TypeAuthorized Distributor
Product OriginImported
ModelXuri Cell Expansion System W25
PriceUpon Request
Temperature Range15°C–32°C
Working Volume25 L
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BrandCytiva
OriginUSA
Manufacturer TypeAuthorized Distributor
Origin CategoryImported
ModelBioProcess Resin Mixer
PricingUpon Request
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BrandCytiva
OriginSwitzerland
ModelNanoAssemblr™ Ignite™ Instrument
Flow Rate Range20–200 mL/min
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BrandCytiva
OriginSweden
ModelÄKTA flux s
Application ScopeResearch & Membrane Screening
Control ModeAutomated Endpoint Control, Constant Retentate Volume (CRV) Mode
User Interface7-inch High-Resolution Touchscreen with Real-Time Process Monitoring
Data HandlingOnboard Logging (CSV Export), Audit-Trail-Ready Event History
Compliance ContextDesigned for GLP-compliant workflows
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BrandCytiva
OriginManufactured in China under Cytiva’s global quality system
Manufacturer TypeAuthorized Distributor
ModelAgile flux TFF Systems
PricingAvailable upon request
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BrandCytiva
OriginSweden
ModelÄKTA flux 6
Application ScopeProcess Development & Small-Scale Production
Control ModeAutomated Endpoint & Constant Retentate Volume (CRV)
Data HandlingReal-Time Logging with Audit-Trail-Capable Software
Regulatory ComplianceDesigned for GMP Environments
Installation & QualificationIQ/OQ Support Available by Certified Engineers
User InterfaceIntegrated Touchscreen HMI
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BrandCytiva
OriginUSA
Manufacturer TypeAuthorized Distributor
Product CategoryImported
ModelXcellerex XDR-50 MO
Application DomainMicrobial Fermentation
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BrandCytiva
OriginSweden
ModelSTF-IRc
Tube OD CapacityUp to 22.2 mm
Automation LevelFully Automated
Sterility AssuranceValidated Aseptic Connection without Biosafety Cabinet
Application DomainBioprocessing Fluid Transfer
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BrandCytiva
OriginUSA
Manufacturer TypeAuthorized Distributor
Product CategoryImported
ModelXcellerex XDR 50–2000
Working Volumes50 L, 200 L, 500 L, 1000 L, 2000 L
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BrandCytiva
OriginSweden
ModelWave Mixer
TypeSterile, Non-invasive Oscillatory Mixing System
CapacityUp to 10 L
Mixing Time≤6.5 s for full homogenization
Drive MechanismProgrammable Rocking Platform with Sinusoidal Motion Profile
Sterility AssuranceDesigned for use with single-use bioprocess bags (e.g., Cytiva HYPERSTACK®, Xcellerex™ XDR bags)
ComplianceCompatible with ISO 13485–certified manufacturing environments and supports GMP-aligned process validation
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BrandCytiva
OriginUnited Kingdom
Manufacturer TypeAuthorized Distributor
Product CategoryImported
ModelGE ReadyToProcess WAVE 25 Bioreactor
Temperature Range6–60 °C
Working Volume Range10–2000 L
Number of Vessels1
Construction MaterialStainless Steel
Sterilization MethodSingle-Use Bioreactor System
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