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ISO 16232: Cleanliness as a Quality Factor in Medical Technology
Particulate contaminants can impair the function of sensitive medical devices. Our latest technical article shows how ISO 16232 helps to reliably define and verify cleanliness requirements.
Clean components are an important prerequisite for the safety and functionality of medical devices. But what requirements does ISO 16232 set for testing and evaluating particulate cleanliness?
In the latest technical article in medizin&technik, STÜKEN MEDICAL demonstrates how the standard can be applied in a practical manner and which aspects should be considered early on in product development.
Read the full article in medizin&technik. PDF
