PTFE Filter 01018-22707: Reliability and Precision for Medical LC Analyses
The PTFE filter 01018-22707 has been specifically developed for the pump modules of Agilent 1260 Infinity LC systems. In the medical field, where rigorous analysis is essential for diagnosis and treatment decisions, this component is vital for maintaining the quality of results. It is used in preventive maintenance for isocratic, binary and quaternary configurations, ensuring the continuity and reliability of the analytical flow.
Strategically placed in the pump system, this filter blocks particles that could cause premature wear or malfunction of internal components such as pistons or valves. Its effectiveness is particularly relevant in hospital laboratories, medical biology centres and clinical research facilities, where even the slightest contamination can distort results.
Made from polytetrafluoroethylene (PTFE), a material known for its chemical stability, the 01018-22707 filter is resistant to a wide range of solvents used in liquid chromatography. This compatibility ensures high-performance, long-lasting filtration without compromising sample or system integrity. Its use helps prevent costly service interruptions while maintaining optimal analysis accuracy.
Adopted in Agilent's recommended standard maintenance procedures, this filter is an essential component for maintaining the performance of LC systems in demanding medical environments. Its use guarantees the reliability of the data generated, while ensuring the longevity of the equipment.
This filter also plays an indirect but crucial role in reducing the costs associated with corrective maintenance operations. By protecting the sensitive components of the liquid chromatography system, it limits the need for unplanned repairs and improves the overall availability of the equipment. This is particularly beneficial in medical facilities with high analytical activity, where any downtime can cause delays in critical analyses.
The 01018-22707 filter also helps maintain stable flow and pressure in the LC system, which are essential parameters for ensuring reproducible results, particularly in standardised or accredited protocols. The integration of this component into a structured preventive maintenance plan makes it possible to anticipate progressive deterioration that could adversely affect the overall performance of the instrumentation.
