Dry Microbial Penetration Performance Tester Operation

  Advantages and characteristics:


  1.Have a strong after-sales service team;


  2.Able to handle various issues in a timely and fast manner,relieving customers of any worries they may have;


  3.Complete spare parts to solve the problem of long lead times when ordering spare parts;


  4.Keep up with industry standards updates and provide textile testing instruments that meet the new standards in a timely manner.


  G287 Dry Microbial Penetration Performance Tester is mainly used to measure the bacterial penetration performance on dry particles within a large or small range of human dandruff material impedance.


  Compliant with standards:


  ISO 22612 Test method for dry microbial penetration of infectious agent protective clothing


  YY/T 0506.5-2009 Surgical sheets,surgical gowns,and clean clothing for patients,medical staff,and instruments Part 5:Test method for dry microbial penetration

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  Operation:


  1.Firstly,prepare the accessories and test samples;


  2.Turn on the power switch of the instrument and enter the LCD screen display interface;


  3.Set parameters such as vibration frequency and operating time;


  4.Turn on the lighting and sterilization for sterilization treatment;


  5.Cut sterile samples into dimensions of 20 centimeters by 20 centimeters and place them in the test container;


  6.Cover the sample with a lid and push it down with a piston to control the degree of relaxation of the sample;


  7.Add about 0.5 grams of bacterial sliding powder;


  8.Insert the culture dish into the narrow opening at the bottom of the container;


  9.Use adhesive tape to seal the top and sides of the narrow opening;


  10.Fill 5 containers with talcum powder,and do not add talcum powder to the 6th container;


  11.Place 6 testers into the instrument testing platform;


  12.Click on[Start]on the screen;


  13.Run at a frequency of 20800 per minute for 30 minutes;


  14.Automatically stop at the set time and remove the container;


  15.Tear off the tape,remove the culture dish,and incubate it in a 35 degree Celsius environment for 24 hours.Count the bacterial colonies in the row,and the effective sample should be a reference dish with a reading of 0.Otherwise,it indicates external contamination,and the experiment should be terminated;


  16.Repeat the above experimental steps and test at least two sets.Calculate the average of 10 valid results as the final result.