Sartopore® Platinum | Midicaps® | 0.2µm | Size 8 | 4pc.

  • Effective Filtration Area: 0.13 m² | 1.4 ft²
  • Pore Size: 0.45 µm prefilter | 0.2 µm final filter
  • Connectors: Inlet: Sanitary ¾“ | Outlet: Sanitary ¾“
  • Sterilization: Delivered sterile (autoclaved)
  • Membrane Material: Modified Polyethersulfone
  • Pack Size: 4 pieces

________________________

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

Filter Size
Sterilization Method
Connector(s)
Price (USD):
$1,270.00
Item No.: 
5495307H8--FF--A
Availability: 
Pieces
4

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

  • Lowest protein adsorption – maximizing product yield
  • Excellent wettability – up to 95% less water needed
  • No wetting issues during integrity testing – preferred for single-use assemblies
  • High chemical compatibility (pH 1-14)
  • Temperature stable
  • Highest effective filter area (1 m2/10”) – less filter consumption
  • Low Extractables Level
  • Reliable Integrity Testing

Application

Typical filtration applications include:

  • Therapeutica
  • Biological Fluids
  • Injection solutions
  • Media
  • Buffer
  • Chemical solutions
  • Cleaning agents and disinfectants

Membrane

Sartopore® Platinum uses a heterogeneous double membrane made of hydrophilized polyethersulfone, which is characterized by high performance data, excellent wettability, high chemical compatibility, high temperature stability and low protein absorption.

New surface coating

A new hydrophilization process has been developed to permanently modify the membrane surface. In this process, a thermally extremely stable and hydrophilic polymer is applied directly to the entire surface of the membrane. This technology creates the membrane properties that are responsible for the exceptionally good wettability and low protein binding of Sartopore® Platinum, even after extreme chemical and thermal stress. As a result, multiple evaporation cycles in dry and wet conditions and in both directions are possible without negative consequences in terms of wettability and integrity testing.

Compatibility

Sartopore®Platinum filters have been developed for sterilization using autoclaving at 134°C | 2bar. The polyethersulfone membrane used is suitable for the filtration of liquids in the pH range of pH 1-14. Therefore, Sartopore® Platinum filters are suitable for most filtration applications in the pharmaceutical and biotechnology sectors.

Excellent wettability

Sartopore® Platinum filters are very easy to wet with the inset of very small amounts of medium. Less than 1 litre of WFI is required to reliably wet a MidiCaps® height 9 (0.26 m²) and then test it for integrity. Due to the excellent wettability, WFI consumption can be significantly reduced, which significantly reduces filtration costs.

Reliable Integrity Testing

Insufficient wetting is one of the main reasons for failing filter integrity tests. In such a case, the affected filter must be rewetted and tested. In addition to the additional costs for the additional tests, there is the risk of losing an entire production batch in the event of repeated failures. The excellent wetting behavior of Sartopore® Platinum helps to eliminate this risk. The use of Sartopore® Platinum results in unprecedented reliability in integrity testing.

Cost savings:

The use of disposable filter elements eliminates the need to invest in stainless steel filter housings. Additional costs for housing cleaning and cleaning validation are eliminated.

Flexibility

Sartopore® Platinum filters are available in a wide range of filtration areas from 4.5 cm² up to 3.0 m² and with a variety of commonly used connections to ensure easy integration into your process regardless of batch size.

Scale Up:

Due to the identical performance data of the different heights in relation to square meters of filter area, Sartopore® Platinum filters are perfectly scalable from small scales to large production scales.

Quality:

Every single element is tested for integrity to meet the highest quality requirements.

Microbial Retention

Sartopore® Platinum filters are validated as sterile filter cartridges according to HIMA and ASTM F-838-05 guidelines.

Documentation:

Sartopore® Platinum filter filters have been designed, developed and produced in accordance with the ISO 9001 certified quality management system. A validation manual is available in accordance with regulatory requirements.

Applications

  • Application
    Single Use Processing
  • Industry
    Pharma / Biotech
  • Modality
    • Form & Fill
    • Buffer & Auxiliaries Filtration
  • Scale
    Production | Small Scale

Biological Information

  • Bacterial Retention
    Quantitative Retention of 1 × E7 CFU/cm² Brevundimonas Diminuta ATCC® 19146 per ASTM methodology

Compliance Information

  • Bacterial Endotoxins
    < 0.25 EU/mL as determined by the LAL test
  • Biological Reactivity
    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".

Connections (Physical)

  • Connector Inlet
    3/4" Tri-clamp 25 mm
  • Connector Outlet
    3/4" Tri-clamp 25 mm
  • Connector(s)
    Inlet: ¾" Sanitary | Outlet: ¾" Sanitary

Dimensions

  • Filter Size
    size 8 (0.13 m² / 1.4 ft²)
  • Filtration Area
    1 m²
  • Outer Diameter
    108.5 mm (77 mm without Connection / Valves)

General Specifications

  • Capsule/Cartridge Format
    Midicaps®
  • Filter Format
    Capsules
  • Maximum Allowable Back Pressure
    2 bar (29 psi) at 20°C; 1.5 bar (21.8 psi) at 50°C
  • Maximum Diffusion
    5 mL/min at 2.5 bar | 36 psi
  • Minimum Required Bubble Point
    3.5 bar | 51 psi
  • Vent Valve
    Standard

Materials of Construction

  • Filter Material
    Polyethersulfone (PES)
  • Housing Material
    Polypropylene (PP)
  • Material o-ring | seal
    Silicone (SI)
  • Membrane Material
    Polyethersulfone, Hydrophobic (PES)

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
    0.45 µm

Product Information

  • Brand
    Sartopore® Platinum
  • Pack Size
    4

Sterility/Purity

  • Delivery Condition
    Sterile - Autoclaved
  • Sterilization Method
    Autoclavable

Usage Protocols

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