Bag-Loop-Assembly
Sartocon® Self Contained Filter and Bag Loop Assemblies are supplied sterile and ready to use. Due to the fully enclosed design the assembly is well suited for vaccine, recombinant protein and highly toxic ADC production.
Item no.: SFA-SUM1467921
Availability (ex works): On Request
Choose your Sartocon® Single-Use Filter Assemblies
The gamma sterilized bag loop assembly consists of a Polyethersulfone membrane (PESU) self contained filter unit, tubing, four pressure domes, retentate and permeate flow meters, two valve bodies for back pressure control in the retentate and permeate line, perestaltic pump tubing and a 10 L recirculation bag including a thermowell and a vent filter.
Bag loop assemblies for the SARTOFLOW® Alpha plus SU are supplied sterile and ready to use. Due to the fully enclosed design the assembly is well suited for vaccine, recombinant protein and highly toxic ADC production. All product wetted parts of the system are supplied sterile and made from single use components. The system is suitable for use in cGMP environments for process development, clinical trials and for small-scale production batches. The cassette is designed with the same hydrodynamic flow path as our larger production scale filter cassettes, enabling linear scale-up to larger filter areas. The single use concept is an ideal choice for Contract Manufacturers, research and development applications and all companies with multiproduct through-put.
Retention Rate
Polyethersulfone membrane (PESU) ultrafiltration Bag Loop Assemblies are available in the following nominal molecular weight cut-offs: 10 kD, 30 kD, 100 kD and 300 kD.
Available Sizes
Sartorius Stedim Biotech Sartocon® Slice Bag Loop Assemblies are availabe in 1, 2 or 3 stack format.
Required Filterholder
Sainless Steel hydraulic and manual holder available.
Filtration Area
Filter area 0.14 m², 0.28 m², 0.42 m²
Datasheet
User Manual
Applications
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IndustryPharma/Biotech
Compliance Information
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BiosafetyAll materials of this filter element meet the requirements of the current USP Biological Reactivity tests for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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ExtractablesThe total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".
Dimensions
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Filtration Area0.28 m²
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Flow Channel GeometryProtein conc. <20% /or viscosity max.3cp
General Specifications
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Cassette FormatSlice Cassettes
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Filter ClassUltrafilter
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Filter FormatCassettes
Materials of Construction
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Integral FramePolypropylene (PP)
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Membrane MaterialPolyethersulfone (PES)
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Sealing CompoundSilicone Grey
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SpacerPolypropylene (PP)
Operating Conditions
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Maximum Inlet Pressure3 bar
Physicochemical Information
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MWCO300 kD
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Non-Fiber ReleasingThis filter product complies with the title 21 of the Code of Federal Regulations (CFR), section 210.3(b)(6) and 211.72.
Product Information
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Filter TypeCrossflow Filters
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Primary Product TypeFilters