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¹Ì±¹ FDA ½ÃÇè±â°ü (U.S.A FDA TESTER)
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½ÄÇ° »ý»ê°úÁ¤¿¡¼ ¿À¿°µÈ ½ÄÇ°À¸·Î ±â¾÷ÀÇ Á¸Æä°¡ °É¸± ¼ö ÀÖ´Â ¾öû³ ¼Õ½ÇÀ» ¿¹¹æÇÏ°í, °ü¸®Çϱâ À§ÇÏ¿©, º» ±â¼úÀÇ µµÀÔÀ» ±ÇÀåÇÕ´Ï´Ù.
Æ®¶óÀÌÅ×Å© ¿¬±¸¼ÒÀÇ º¸°í¼: ¹Ì ½ÄÇ°ÀǾ౹: 1058842/ORL ½ÃÇè¹øÈ£: 98-10-320Report from Tri-Tech Laboratories, Inc., FDA--1058842/ORL Test # 98-10-320Purpose: Disinfectant Validation Process Results: The concentration of bacteria recovered from all inoculated treated samples show a 3-5 log reduction. This factor proves that the disinfection process utilized in this study is effective in inhibiting the most common bacterial problems in producing a high quality product. The concentration of E. Coli 0157 bacteria recovered after only one (1) minute of exposure to the plasma show a 5 log (99.999%) reduction.Purpose: Disinfectant Validation Process½ÃÇè¸ñÀû: »ì±Õ·Â °ËÁõ È®ÀÎ °úÁ¤Results: The concentration of bacteria recovered from all inoculated treated samples show a 3 - 5 log reduction.
This factor proves that the disinfection process utilized in this study is effective in inhibiting the most common bacteria problems in producing a high quality product.The concentration of E-coil 0157 bacteria recovered after only one(1) minute of exposure to the Biozone show a 5 log (99.999%) reduction½ÃÇè°á°ú: »ùÇ÷Π¸ðµÎ ¹è¾çµÈ ¼¼±ÕÀº ±× ³óµµ°¡ ÃæºÐÈ÷ ȸº¹µÇ¾ú°í 3-5log(99.9-99.999%)·Î °¢°¢ °¨¼ÒµÇ´Â °ÍÀ» È®ÀÎÇÏ¿´½À´Ï´Ù.ÀÌ ½ÃÇè¿¡ ÀÌ¿ëµÈ »ì±Õ °úÁ¤Àº °íÇ°ÁúÀÇ Á¦Ç°À» »ý»êÇÏ´Â °÷¿¡¼ °øÅëÀûÀ¸·Î ¹ß»ýÇÏ´Â ¼¼±Õ ¹®Á¦µéÀ» ¾ïÁ¦Çϴµ¥ È¿°úÀûÀ̶ó´Â °ÍÀ» Áõ¸íÇÏ¿´½À ´Ï´Ù.
O-157 ¼¼±ÕÀÇ ³óµµ¸¦ ȸº¹½ÃÄÑ ´ÜÁö 1ºÐ °£ ³ëÃâ½ÃÄÑ 5logÀÎ 99,999%·Î ¼¼±ÕÀÌ °¨¼ÒÇÏ´Â °ÍÀ» È®ÀÎÇÏ¿´½À´Ï´Ù.