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PubMed

Comparison of two models of biofilm formation on reusable stainless steel medical device material.

PMID: 41265798 ·

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RevistaThe Journal of hospital infection
Ano
PMID41265798

Resumo

Reusable medical devices require reprocessing before subsequent patient use. Inadequate reprocessing can create suitable conditions for contaminating microbes to form biofilm. Despite this threat, there is a lack of guidance for medical device manufacturers to make biofilm assessment on their device labelling and instructions for use. Currently, there are no US Food and Drug Administration-recognized standardized models for biofilm formation on medical devices or device materials. To assess esta

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