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Sartopore® 2 SartoScale Disposable

Sartopore® 2 is the industry standard of high-performance polyethersulfone (PES) liquid filters. A broad variety of different pore size combinations ensures highly economic and safe filtration performance. From single-layer high flow solutions to specific Mycoplasma retentive filters, Sartopore®2 perfectly adapts to your specific process needs.

Order Number:  5445307GS--HH--M

Availability:  On Request

Sterilizing-Grade, 0.2 µm Rated Filters
Sartopore®2 HF Pore size: 0.2 µm (single layer)
Sartopore®2 Pore size: 0.45 | 0.2 µm (heterogeneous PES double layer)
Sartopore®2 XLG Pore size: 0.8 | 0.2 µm (heterogeneous PES double layer)
Sartopore®2 XLI Pore size: 0.35 | 0.2 µm (heterogeneous PES double layer)

It is the identical final 0.2 µm membrane layer which ensures sterility of your product. But it is the pre-filter porosity which makes the difference. Depending on specific product properties a finer or coarser pre-filter layer can significantly improve the capacity of the filter. Quasi particle-free liquids like buffer solutions can be filtered without any pre-filter layer for increasing the flow performance.
If a new process is designed or existing processes are optimized, Sartopore® 2 allows cost reduction of up to 90%. The best-performer of your specific application can be easily identified by Increase® filterability trials. Make use of this service to understand the benefit for your filtration process.
Your Benefits:

  • Lowest filtration costs (highest filter capacity)
  • Various filter solutions within one platform (identical materials used for your process)

Mycoplasma-Retentive, 0.1 µm Rated Filters
Sartopore®2 XLM Pore size: 0.2 | 0.1 µm (heterogeneous PES double layer)
It is well known that Mycoplasma can be present in commercially available cell culture media. Because Mycoplasma are able to penetrate 0.2 µm rated sterile filters, the industry specifically developed finer filter membranes (0.1 µm) for the successful retention of Mycoplasma.
It is the highly asymmetric structure and the perfect fit between the 0.2 µm prefilter layer and the 0.1 µm final membrane which ensures an unmet combination of highest safety and highest filtration capacity. Sartopore® 2 XLM is the most powerful filter in the market and is fully validated as sterilizing grade filter (according to ASTM…) and Mycoplasma removal.
Your Benefits:
  • Lowest filter consumption by high filtration capacity
  • Lowest risk of Mycoplasma contamination for you fermentation process
  • Perfect fit to Sartopore® 2 used in other process steps

Bioburden Reduction, 0.45 µm Rated Filters
Sartopore®2 Pore size: 0.8 | 0.45 µm (heterogeneous PES double layer)
Sartopore®2 0.45 µm rated filter cartridges are designed for bioburden reduction and particle removal from a broad range of pharmaceutical products. They offer extremely high flow rates and total throughputs and are therefore ideally suited for membrane prefiltration of aqueous solutions and highly viscous, difficult to filter pharmaceutical products.
For highest process flexibility all Sartopore®2 filters are available for conventional or single use applications. All filter elements are available in various sizes and adapter combinations. Please review the selection guide in the supporting resources literature.

Datasheet

SartoScale — Filter Test Disposables for Use in the Biopharmaceutical Industry
en 461.9 kB

User Manual

SartoScale Filter Test Disposables — Bedienungsanleitung für SartoScale Filter Test Disposables
en 80.3 kB

Product properties

  • Filter Type
    Flat disc Capsules
  • Type
    Sterile filter
  • Membrane filter material
    Polyethersulfone (PES)
  • Membrane material
    Polyethersulfone (PES)
  • Filtration area
    17.3 cm²
  • Branch
    Pharma / Biotech

Technical attributes

  • Sterilization Procedures
    Autoclaving=== 1 cycle at max. 134 °C, 2 bar | 29 psi, 30 min.
  • Bacterial Endotoxins
    < 0.18 EU/mL as determined by the LAL test
  • GMP Compliance
    This product was manufactured in conformance with established Current Good Manufacturing Practice (cGMP) standards.
  • Maximum Differential Pressure
    20 °C=== 5 bar; 80 °C=== 2 bar
  • Biosafety
    All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
  • Extractables
    The total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".
  • Non-Fiber Releasing
    This filter product complies with the title 21 of the Code of Federal Regulations (CFR), section 210.3(b)(6) and 211.72.
  • Housing material
    Polypropylene (PP)
  • Min. required Bubble Point
    3.2 bar | 46 psi

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