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  • Sartopore® 2 | 0.2 µm | Midicaps®

Sartopore® 2 Midicaps® 0.2µm size 0 | 2pc

Tech Support Documents
Sartopore® 2 Midicaps® 0.2µm size 0 | 2pc Sartopore® 2 Midicaps® 0.2µm size 0 | 2pc Sartopore® 2 Midicaps® 0.2µm size 0 | 2pc
 

  • Effective Filtration Area: 0.05 m² | 0.5 ft²
  • Pore Size: 0.45 µm prefilter | 0.2 µm final filter
  • Sterilization: Delivered sterile (Autoclaved)
  • Membrane Material: Polyethersulfone
  • Pack Size: 2 pieces

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Connector explanation:

O = Hose Barb ½“ | S = Sanitary 1 ½“ | H = Hose Barb ¼“ | F = Sanitary ¾“

Size explanation:

Size 7 = 0.065 m² | Size 8 = 0.13 m² | Size 9 = 0.26 m² | Size 0 = 0.52 m²

Item No.: 
5445307H0--SF--V
Availability: 

*Custom/bulk order quotes are provided within 72 hours of request.

Sartopore ® 2 Membrane Filters Midicaps are self-contained, ready-to-use, sterile filter elements for sterile filtration in the pharmaceutical | pharmaceutical Biotech industry Due to its hydrophilic, heterogeneous, double-layer polyethersulfone membrane, Sartopore 2 capsules are designed for the sterile filtration of a diverse bandwidth of pharmaceutical products.

  • Single-use Midicaps® for process scale
  • Reduce cleaning and cleaning validation
  • Superior Flow Performance & Service Life
  • Most economical process solution
  • Broad chemical compatibility

Applications

Typical applications include the sterile filtration of: therapeutics - biological liquids - injection solutions - media - buffers - chemicals - cleaning and disinfecting agents.

Compatibility

The polyethersulfone membrane is compatible in a range of pH 1 to 14, making the Sartopore® 2 Midicaps® ideal for the filtration of solutions with low | high pH.

Easy handling

Sartopore® 2 Midicaps® are supplied as individually sterile-packaged, ready-to-use units, eliminating the need for pre-application sterilization.

Flexibility

Sartopore® 2 0.2 μm Midicaps® are supplied with different filtration areas of 500 cm² | 0.5 ft² to 0.45 m² | 5 ft² for easy adaptation to every filtration process regardless of batch size.

Scalability

Consistent and predictable scale-up and scale-down processes can be operational because all Sartopore® 2 Midicaps® are manufactured using the same membrane types and identical construction materials.

Cost savings

The use of single-use filter elements does not require investment in stainless steel filter housing. Eliminates additional costs for housing cleaning and cleaning validation.

Microbiological Retention

Sartopore® 2 Midicaps® 0.2 μm are fully validated sterile filter elements, in compliance with HIMA and ASTM F-838-05 guidelines.

Quality

Every single element is integrity checked to meet the highest quality standards.

Documentation

Sartopore® 2 Midicaps® are designed, developed and manufactured in accordance with iso 9001 certified quality management system. A Validation Manual is available in accordance with regulatory requirements.

User Manual

Directions for Use - Standard Filter Cartridges and Mini Cartridges
en 326.3 kB

Applications

  • Industry
    Pharma / Biotech

Compliance Information

  • Bacterial Endotoxins
    < 0.25 EU/mL as determined by the LAL test
  • Extractables
    The total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".

Connections (Physical)

  • Connector Inlet
    1.5" Sanitary
  • Connector Outlet
    3/4" Sanitary

Dimensions

  • Filter Size
    size 0 (0.45 m² / 4.8 ft²)
  • Outer Diameter
    108.5 mm (77 mm without Connection / Valves)

General Specifications

  • Capsule/Cartridge Format
    Midicaps®
  • Maximum Allowable Back Pressure
    • 2 bar (29 psi) at 20°C
    • 1.5 bar (21.8 psi) at 50°C
  • Maximum Diffusion
    at 20 °C and 2.5 bar | 36 psi: 0.065 m² | 0.7 ft²: 5 mL/min; 0.13m² | 1.4 ft²: 6 mL/min; 0.26 m² | 2.8 ft²: 9 mL/min; 0.52 m² | 5.6 ft²: 18 mL/min
  • Minimum Required Bubble Point
    3.2 bar | 46 psi

Materials of Construction

  • Material o-ring | seal
    Silicone (SI)
  • Membrane Material
    Polyethersulfone (PES)
  • Support Fleece
    Polyester (PET)

Operating Conditions

  • Maximum Differential Pressure
    20 °C: 5 bar, 50 °C: 3 bar
  • Maximum Operating Pressure
    5 bar (72.5 psi)

Physicochemical Information

  • 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.
  • Pore Size Final-filter
    0.2 μm
  • Pore Size Pre-filter
    0.45µm

Product Information

  • Brand
    Sartopore® 2
  • Pack Size
    2
  • Type
    Size 0 | Connectors: SF

Sterility/Purity

  • Delivery Condition
    Sterile - Autoclaved
  • Sterilization Method
    Autoclavable

Usage Protocols

  • Sterilization Procedures
    Autoclaving: at 134°C, 30 min, 2 bar, min. 25 Cycles