TS EN ISO 23328-2 Inhalation System Filters for Respiratory and Anesthetic Use - Part 2: Non-Filtration Related Properties

Respirator Compatibility Tests

TS EN ISO 23328-2 Inhalation System Filters for Respiratory and Anesthetic Use - Part 2: Non-Filtration Related Properties

The BS EN 23328-2 standard was developed by the British Standards Institute (BSI), which describes the non-filtration properties of the respiratory system filters used in respiratory and anesthetic devices. This standard has been published in our country by the Turkish Standards Institute (TSE) with the following title: TS EN ISO 23328-2 Respiratory system filters for anesthesia and respiratory use - Part 2: Non-filtering issues. This standard was later published by the International Standards Organization (ISO).

TS EN ISO 23328-2 Inhalation System Filters for Respiratory and Anesthetic Use - Part 2: Non-Filtration Related Properties

This standard covers the rules for non-filtering properties of respiratory system filters designed for use in anesthesia and breathing, and describes information on connection inlets, leakage, flow resistance, packaging and marking. This part of the TS EN ISO 23328 standard provides requirements for non-filtering aspects of respiratory system filters.

These filters are used to reduce various particles, including microorganisms in the gases returned and returned to patients. The first part of the TS EN ISO 23328 standard describes a test method for evaluating the filtration performance of the respiratory filter.

The TS EN ISO 23328-2 standard addresses the connection ports of the filters, leakage, flow resistance, packaging, marking and the information provided. The test method is designed for respiratory filters used with a clinical respiratory system. Filters designed to protect vacuum sources or gas sample lines, filter compressed gases, or protect test equipment for physiological breathing measurements are covered by this standard.

Briefly, respiratory and anesthetic filters ensure that patients are protected against cross contamination during anesthesia and ventilation.

Within the scope of breathing apparatus compatibility tests carried out by our organization EUROLAB, testing services in accordance with TS EN ISO 23328-2 standard are also provided.

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