Bioburden Testing - European Biomedical Institute

	Turnaround time:	4 weeks

	Sample requirements:	3 test items (non-sterile)

ISO 11737-1 & USP <61>
	The scope of the study included determining the bioburden of the test articleaccording to ISO 11737-1:2018 Sterilization of healthcare products – Microbiological methods – Part 1: Determination of a population of microorganism on products. The aim of the study is to determine the bioburden of the medical device.

	Bioburden of test item is assessed by removing microorganisms from test item surface followed by their culturing and enumeration.