Sartorius Lab Instruments - Sartopure GF Plus MidiCap 0.65µm Filter BH9. 4pcs

• Prefiltration of cell culture media and buffers in biopharmaceutical production.
• Clarification of fermentation broths and other biological fluids.
• Protection of downstream sterile filters and chromatography columns.
• Reduction of particulate load in laboratory-scale processes.
• Use in pilot-scale and small-batch bioprocessing operations.

Filter Type

Sartopure GF Plus MidiCap, typically a pleated glass fibre depth filter.

Pore Size

0.65 µm, designed for effective particle retention and clarification.

Housing Material

Commonly polypropylene or similar inert polymer, suitable for bioprocessing.

Connection Type

Typically hose barb or sanitary flange connections, depending on the MidiCap size.

Typical Flow Rate

Varies significantly with differential pressure and fluid viscosity; consult datasheet for specific performance curves.

Sterilisation

Units of this type are commonly autoclavable or can be sterilised by gamma irradiation.

Effective Filtration Area

For MidiCaps, this typically ranges from 0.05 m² to 0.2 m², influencing throughput.

• What is the primary benefit of using a glass fibre filter like the Sartopure GF Plus?

  Glass fibre filters offer high dirt-holding capacity and excellent flow rates, making them ideal for prefiltration applications where high particulate loads are present.

• Can these filters be used for sterile filtration?

• Are these filters suitable for single-use applications?

• What kind of fluids can these filters process?

• How many filters are included in this listing?

Laboratory filtration systems are valued for reliability and durability, making them suitable for used purchase when sourced carefully. Buyers typically prioritise checking membrane and filter condition, as replacement costs can be significant. Industry sentiment favours systems from established manufacturers known for consistent performance. Common strengths include robust construction, compatibility with various applications, and availability of spare parts. When assessing used units, verifying maintenance history and operational specifications remains essential for ensuring continued performance in biotech and pharmaceutical environments.

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