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 ‫ﺍﻧﺘﺒﺎﻩ‬

‫ﺣﻘﻮﻕ ﺍﻟﻄﺒﻊ ﻭﺍﻟﻨﺸﺮ ﻟﻬﺬﺍ )"ﺍﻟﻤﺸﺎﺭ ﺇﻟﻴﻬﺎ ﻓﻴﻤﺎ ﻳﻠﻲ ﺑﺎﺳﻢ "ﺷﺮﻛﺘﻨﺎ( ‪ .Beijing Aeonmed Co., Ltd‬ﺗﻤﺘﻠﻚﺷﺮﻛﺔ‬

‫ﺍﻟﺪﻟﻴﻞﺍﻟﻤﻨﺸﻮﺭ ﻏﻴﺮ ﺍﻟﻌﺎﻡ‪ ،‬ﻭﺗﺤﺘﻔﻆ ﺑﺤﻘﻮﻕ ﺍﻻﺣﺘﻔﺎﻅ ﺑﻪ ﻛﻮﺛﻴﻘﺔ ﺁﻣﻨﺔ‪ .‬ﺭﺍﺟﻊ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ ﻋﻨﺪ ﺗﺸﻐﻴﻞ ﺍﻟﻤﻨﺘﺠﺎﺕ ﻭﺻﻴﺎﻧﺘﻬﺎﻭﺇﺻﻼﺣﻬﺎ‬

‫‪.‬ﻓﻘﻂ‪ .‬ﻳﺤﻖ ﻟﺸﺮﻛﺘﻨﺎ ﻓﻘﻂ ﻣﻨﺢ ﺍﻹﺫﻥ ﺑﺎﺳﺘﺨﺪﺍﻡ ﻫﺬﻩ ﺍﻟﻮﺛﻴﻘﺔ ﺃﻭ ﻧﺴﺨﻬﺎ ﻟﻶﺧﺮﻳﻦ‬

‫ﻳﺘﻢﺗﻀﻤﻴﻦ ﺍﻟﻤﻮﺍﺩ ﺍﻟﻤﺴﺠﻠﺔ ﺍﻟﻤﻠﻜﻴﺔ ﻭﺍﻟﻤﺤﻤﻴﺔ ﺑﻤﻮﺟﺐ ﻗﺎﻧﻮﻥ ﺣﻘﻮﻕ ﺍﻟﻄﺒﻊ ﻭﺍﻟﻨﺸﺮ ﻓﻲ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ‪ .‬ﻻ ﻳﺠﻮﺯ ﻧﺴﺦ ﺃﻱ ﻗﺴﻢﻣﻨﻪ ﺃﻭ ﻧﺴﺨﻪ ﺃﻭ‬

‫‪.‬ﺗﺮﺟﻤﺘﻪ ﺇﻟﻰ ﻟﻐﺎﺕ ﺃﺧﺮﻯ ﺩﻭﻥ ﺍﻟﺤﺼﻮﻝ ﻋﻠﻰ ﻣﻮﺍﻓﻘﺔ ﻛﺘﺎﺑﻴﺔ ﻣﺴﺒﻘﺔ ﻣﻦ ﺷﺮﻛﺘﻨﺎ ﺍﻟﺘﻲ ﺗﺤﺘﻔﻆ ﺑﺤﻘﻮﻕﺍﻟﻄﺒﻊ ﻭﺍﻟﻨﺸﺮ‬

‫ﻳﻌﺘﺒﺮﻛﻞ ﻣﺎ ﻫﻮ ﻣﻜﺘﻮﺏ ﻓﻲ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞﺻﺤﻴﺤًﺎ‪ ،‬ﻭﻟﻜﻨﻪ ﻟﻴﺲﺑﺪﻳﻼً ﻋﻦ ﻣﻤﺎﺭﺳﺔ ﺍﻟﺤﻜﻢ ﺍﻟﻤﻬﻨﻲ‪ .‬ﺷﺮﻛﺘﻨﺎ ﻟﻴﺴﺖ ﻣﺴﺆﻭﻟﺔ ﻗﺎﻧﻮﻧًﺎﻋﻦ ﺃﻱ ﺃﺧﻄﺎء‬
‫ﻣﻄﺒﻮﻋﺔ ﺩﺍﺧﻞ ﻭ‪/‬ﺃﻭ ﺃﻱ ﺃﺿﺮﺍﺭ ﻧﺎﺟﻤﺔ ﻋﻦ ﺍﻟﺘﻮﺻﻴﻞ ﻭﺍﻟﺘﺸﻐﻴﻞ ﻏﻴﺮ ﺍﻟﺼﺤﻴﺤﻴﻦ ﻟﻠﻤﻌﺪﺍﺕ‪ .‬ﻻ ﺗﻘﺪﻡ‬
‫ﺷﺮﻛﺘﻨﺎﺍﻻﻣﺘﻴﺎﺯﺍﺕ ﺍﻟﺘﻲ ﻳﻤﻨﺤﻬﺎ ﻗﺎﻧﻮﻥ ﺑﺮﺍءﺍﺕ ﺍﻻﺧﺘﺮﺍﻉ ﻷﻱ ﻃﺮﻑ ﺁﺧﺮ‪ .‬ﺷﺮﻛﺘﻨﺎ ﻟﻴﺴﺖ ﻣﺴﺆﻭﻟﺔﻗﺎﻧﻮﻧًﺎ ﻋﻦ ﺍﻟﻨﺘﺎﺉﺞ ﺍﻟﻨﺎﺟﻤﺔﻋﻦ ﺍﻧﺘﻬﺎﻙ‬

‫‪.‬ﻗﺎﻧﻮﻥ ﺑﺮﺍءﺍﺕ ﺍﻻﺧﺘﺮﺍﻉ ﺃﻭ ﺍﻧﺘﻬﺎﻙ ﺣﻘﻮﻕ ﺍﻟﻄﺮﻑ ﺍﻟﺜﺎﻟﺚ‬

‫ﻳﺠﺐﻋﻠﻰ ﺃﻱ ﻣﺴﺘﺨﺪﻡ ﻗﺮﺍءﺓ ﻫﺬﻩ ﺍﻟﻤﻘﺎﻟﺔ ﻗﺒﻞ ﺍﺳﺘﺨﺪﺍﻡ ﻣﻨﺘﺠﺎﺕ ﺷﺮﻛﺘﻨﺎ‪ .‬ﺗﻌﺮﺽ ﻫﺬﻩ ﺍﻟﻤﻘﺎﻟﺔ ﺧﻄﻮﺍﺕ ﺍﻟﺘﺸﻐﻴﻞ ﺍﻟﺘﻲ ﻳﺠﺐﻗﺮﺍءﺗﻬﺎ ﺑﻌﻨﺎﻳﺔ‪.‬‬
‫ﺍﻻﺳﺘﺨﺪﺍﻡ ﻏﻴﺮ ﺍﻟﺴﻠﻴﻢ ﻗﺪ ﻳﻌﺮﺽ ﺍﻟﻤﻌﺪﺍﺕ ﺃﻭ ﺍﻷﺷﺨﺎﺹ ﻟﻠﺨﻄﺮ‪ .‬ﻟﻦ ﺗﺘﺤﻤﻞ ﺍﻟﺸﺮﻛﺔ ﻣﺴﺆﻭﻟﻴﺔ ﺍﻟﺴﻼﻣﺔﻭﺍﻟﻤﻮﺛﻮﻗﻴﺔ ﻭﺍﻷﺩﺍء ﺇﺫﺍ ﺗﻢ ﺍﺳﺘﺨﺪﺍﻡ‬
‫‪.‬ﺍﻟﻤﻌﺪﺍﺕ ﺑﺸﻜﻞ ﻏﻴﺮ ﺻﺤﻴﺢ‪ .‬ﻟﻦ ﺗﻘﺪﻡ ﺍﻟﺸﺮﻛﺔ ﺧﺪﻣﺔ ﻣﺠﺎﻧﻴﺔ ﻟﻠﻤﻌﺪﺍﺕ ﺍﻟﺘﻲ ﻳﺴﺎءﺍﺳﺘﺨﺪﺍﻣﻬﺎ‬

‫ﻳﺤﻖﻟﺸﺮﻛﺘﻨﺎ ﻣﺮﺍﺟﻌﺔ ﺃﻱ ﻣﺤﺘﻮﻯ ﻓﻲ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ ﺩﻭﻥ ﺇﺷﻌﺎﺭ ﻣﺴﺒﻖ؛ ﻭﻟﻴﺲ ﻋﻠﻴﻬﺎ ﺃﻱ ﺍﻟﺘﺰﺍﻡ ﺑﺘﺤﺪﻳﺚ ﺍﻷﺟﻬﺰﺓ ﺃﻭ ﺍﻟﺒﺮﺍﻣﺞﺍﻟﺨﺎﺻﺔ‬

‫‪.‬ﺑﺎﻟﻤﻌﺪﺍﺕ ﺍﻟﻤﻮﺿﺤﺔ ﻫﻨﺎ ﻟﻠﻤﺴﺘﺨﺪﻡ ﺃﻭ ﺍﻟﻤﺎﻟﻚ‬

‫ﺃﻧﺎ‬
 ‫ﺗﺤﺬﻳﺮﻟﻼﺳﺘﺨﺪﺍﻡ‬

‫!ﻣﺮﺣﺒﺎﺑﻜﻢ ﻓﻲ ﺍﺳﺘﺨﺪﺍﻡ ﻣﻨﺘﺠﺎﺗﻨﺎ‬

‫ﻣﻦﺃﺟﻞ ﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﺍ ﺍﻟﻤﻨﺘﺞ ﺑﺸﻜﻞ ﺻﺤﻴﺢ ﻭﻓﻌﺎﻝ‪ ،‬ﻳﺮﺟﻰ ﻗﺮﺍءﺓ ﺗﻌﻠﻴﻤﺎﺕ ﺍﻟﺘﺸﻐﻴﻞ ﻫﺬﻩ ﺑﻌﻨﺎﻳﺔ ﻭﺑﺸﻜﻞ ﻛﺎﻣﻞ ﻗﺒﻞ ﺍﺳﺘﺨﺪﺍﻡﺍﻟﻤﻨﺘﺞ ﻷﻭﻝ‬
‫‪.‬ﻣﺮﺓ‬
‫ﻋﻨﺪﺍﺳﺘﺨﺪﺍﻡ ﺍﻟﻤﻨﺘﺞ‪ ،‬ﺍﺗﺒﻊﺩﺍﺉﻤًﺎ ﺍﻟﻤﻌﻠﻮﻣﺎﺕ ﺍﻟﻮﺍﺭﺩﺓ ﻓﻲ ﺗﻌﻠﻴﻤﺎﺕ ﺍﻟﺘﺸﻐﻴﻞ ﻫﺬﻩ ﻋﻠﻰ ﺃﺳﺎﺱ ﺍﻟﻔﻬﻢ ﺍﻟﻜﺎﻣﻞ ﻟﻠﻤﻌﻠﻮﻣﺎﺕﺍﻟﻮﺍﺭﺩﺓ ﻓﻲ‬

‫‪.‬ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ‬

‫‪.‬ﻫﺬﺍﺍﻟﻤﻨﺘﺞ ﻓﻘﻂﻟﻼﺳﺘﺨﺪﺍﻡ ﺍﻟﻤﻘﺼﻮﺩ ﻛﻤﺎ ﻫﻮ ﻣﻮﺿﺢ ﻓﻲ ﺗﻌﻠﻴﻤﺎﺕ ﺍﻟﺘﺸﻐﻴﻞ ﻫﺬﻩ‬

‫‪.‬ﻳُﺴﻤﺢﻓﻘﻂ ﻟﻤﺤﺘﺮﻓﻲ ﺍﻟﺨﺪﻣﺔ ﺍﻟﻤﺪﺭﺑﻴﻦﺧﺼﻴﺼًﺎ ﺑﺈﺟﺮﺍء ﺗﻮﺻﻴﻞ ﻫﺬﺍ ﺍﻟﻤﻨﺘﺞ ﻭﺻﻴﺎﻧﺘﻪ‬

‫‪.‬ﺑﺎﻟﻨﺴﺒﺔﻷﻱ ﺣﺎﻟﺔ ﻓﻲ ﻋﻤﻠﻴﺔ ﺍﻻﺳﺘﺨﺪﺍﻡ‪ ،‬ﻳﺮﺟﻰ ﺍﻻﺗﺼﺎﻝ ﺑﻨﺎ‪ .‬ﺳﻮﻑ ﻧﻘﺪﻡ ﻟﻚ ﺧﺪﻣﺔ ﺩﺍﻓﺉﺔ‬

‫‪.‬ﻣﻮﺍﺻﻔﺎﺕﺍﻟﻤﻨﺘﺞ ﻋﺮﺿﺔ ﻟﻠﺘﻐﻴﻴﺮ ﺩﻭﻥ ﺇﺷﻌﺎﺭ‬

‫ﺛﺎﻧﻴﺎ‬
 ‫‪:‬ﺍﻟﺸﺮﻛﺔﺍﻟﻤﺼﻨﻌﺔ (ﺍﻟﻤﺎﻟﻚ)‬ ‫ﺷﺮﻛﺔﺑﻜﻴﻦ ﺃﻳﻮﻧﻤﻴﺪ ﺍﻟﻤﺤﺪﻭﺩﺓ‬

‫ﺍﻟﺸﺮﻛﺔﺍﻟﻤﺼﻨﻌﺔ (ﺍﻟﻤﺎﻟﻚ)‬ ‫‪،‬ﺍﻟﻐﺮﻓﺔ‪405,‬ﺍﻟﻄﺎﺑﻖ ﺍﻟﺴﻔﻠﻲ ﻣﻦ ‪ 1‬ﺇﻟﻰ ﺍﻟﻄﺎﺑﻖ ﺍﻟﺮﺍﺑﻊ ﻣﻦ ‪ 901‬ﻭﺣﺪﺓ‬

‫‪:‬ﻋﻨﻮﺍﻥ‬ ‫ﺍﻟﻤﺒﻨﻰ‪ ،9‬ﺭﻗﻢ ‪ 26‬ﺍﻟﻄﺮﻳﻖ ﺍﻟﺪﺍﺉﺮﻱ ﺍﻟﺨﺎﺭﺟﻲ ﺍﻟﻐﺮﺑﻲ‪ ،‬ﻣﻨﻄﻘﺔ‬

‫ﻓﻨﻐﺘﺎﻯ‪،‬ﺑﻜﻴﻦ ‪ ،100070‬ﺍﻟﺼﻴﻦ‬

‫‪:‬ﻣﻨﺸﺄﺓ‬ ‫ﺷﺮﻛﺔﺑﻜﻴﻦ ﺃﻳﻮﻧﻤﻴﺪ ﺍﻟﻤﺤﺪﻭﺩﺓ‬

‫‪:‬ﻋﻨﻮﺍﻥﺍﻟﻤﻨﺸﺄﺓ‬ ‫‪،‬ﺍﻟﻐﺮﻓﺔ‪405,‬ﺍﻟﻄﺎﺑﻖ ﺍﻟﺴﻔﻠﻲ ﻣﻦ ‪ 1‬ﺇﻟﻰ ﺍﻟﻄﺎﺑﻖ ﺍﻟﺮﺍﺑﻊ ﻣﻦ ‪ 901‬ﻭﺣﺪﺓ‬

‫ﺍﻟﻤﺒﻨﻰ‪ ،9‬ﺭﻗﻢ ‪ 26‬ﺍﻟﻄﺮﻳﻖ ﺍﻟﺪﺍﺉﺮﻱ ﺍﻟﺨﺎﺭﺟﻲ ﺍﻟﻐﺮﺑﻲ‪ ،‬ﻣﻨﻄﻘﺔ‬

‫ﻓﻨﻐﺘﺎﻯ‪،‬ﺑﻜﻴﻦ ‪ ،100070‬ﺍﻟﺼﻴﻦ‬

‫ﺭﻗﻢ‪ 10‬ﺷﺎﺭﻉ ﺗﺸﺎﻭﺑﺎﻱ‪ ،‬ﻃﺮﻳﻖ ﻳﻨﺠﺒﻴﻦﻏﺮﺑًﺎ‪ ،‬ﻣﻨﻄﻘﺔ ﻳﺎﻧﺠﻴﺎﻭ‬

‫ﻟﻠﺘﻨﻤﻴﺔ‪ ،065201،‬ﻻﻧﻐﻔﺎﻧﻎ‪ ،‬ﺧﺒﻲ‪ ،‬ﺍﻟﺼﻴﻦ‬

‫‪:‬ﺧﺪﻣﺔ‬ ‫ﺷﺮﻛﺔﺑﻜﻴﻦ ﺃﻳﻮﻧﻤﻴﺪ ﺍﻟﻤﺤﺪﻭﺩﺓ‬

‫‪:‬ﻋﻨﻮﺍﻥﺍﻟﺨﺪﻣﺔ‬ ‫ﺭﻗﻢ‪ 10‬ﺷﺎﺭﻉ ﺗﺸﺎﻭﺑﺎﻱ‪ ،‬ﻃﺮﻳﻖ ﻳﻨﺠﺒﻴﻦﻏﺮﺑًﺎ‪ ،‬ﻣﻨﻄﻘﺔ ﻳﺎﻧﺠﻴﺎﻭ‬

‫ﻟﻠﺘﻨﻤﻴﺔ‪ ،065201،‬ﻻﻧﻐﻔﺎﻧﻎ‪ ،‬ﺧﺒﻲ‪ ،‬ﺍﻟﺼﻴﻦ‬

‫‪:‬ﻫﺎﺗﻒ‬ ‫‪86-10-83681616 +‬‬

‫‪:‬ﻓﺎﻛﺲ‬ ‫‪83681616-8130 -86-10 +‬‬

‫‪:‬ﺧﻂﺍﻟﺨﺪﻣﺔ‬ ‫‪800-810-8333 86 +‬‬

‫‪:‬ﻣﻮﻗﻊﺇﻟﻜﺘﺮﻭﻧﻲ‬ ‫‪http://www.aeonmed.com‬‬

‫‪:‬ﺑﺮﻳﺪﺇﻟﻜﺘﺮﻭﻧﻲ‬ ‫‪Service@aeonmed.com‬‬

‫‪:‬ﺍﻟﻤﻤﺜﻞﺍﻷﻭﺭﻭﺑﻲ‬ ‫‪ AG‬ﻫﺎﻳﺮﺍﻟﻄﺒﻴﺔ‬

‫‪:‬ﻋﻨﻮﺍﻥ‬ ‫ﺷﺎﺭﻉﻛﺎﺭﻝ ﻫﺎﻳﺮ‪ 56130 ،1/3 .‬ﺑﺎﺩ ﺇﻳﻤﺲ‪ ،‬ﺃﻟﻤﺎﻧﻴﺎ‬

‫ﺛﺎﻟﺜﺎ‬
‫ﺭﺍﺑﻌﺎ‬
 ‫ﺟﺪﻭﻝﺍﻟﻤﺤﺘﻮﻳﺎﺕ‬

‫‪1‬‬ ‫‪ ................................................. ..................................................‬ﻣﻘﺪﻣﺔ‬ ‫‪1-1..................‬‬

‫‪ ........................................... .............................................‬ﻣﺴﺆﻭﻟﻴﺔﺍﻟﺸﺮﻛﺔ ﺍﻟﻤﺼﻨﻌﺔ ‪1.1‬‬ ‫‪1-1‬‬
‫‪ .............................................. ........................‬ﻣﺴﺆﻭﻟﻴﺔﺍﻟﻤﺸﻐﻞ ﻋﻦ ﺳﻼﻣﺔ ﺍﻟﻤﺮﺿﻰ ‪1.2‬‬ ‫‪1-1‬‬
‫‪ ................................................. ..................................................‬ﺗﻌﺮﻳﻔﺎﺕ ‪1.3‬‬ ‫‪2-1....................‬‬
‫‪ ........................................... ...........................................‬ﺍﻟﺘﺤﺬﻳﺮﺍﺕﻭﺍﻟﺘﻨﺒﻴﻬﺎﺕ ﻭﺍﻟﻤﻼﺣﻈﺎﺕ ‪1.4‬‬ ‫‪2-1‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺘﺤﺬﻳﺮﺍﺕ‪1.4.1‬‬ ‫‪2-1.................‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺘﺤﺬﻳﺮﺍﺕ‪1.4.2‬‬ ‫‪4-1...................‬‬
‫‪ .............................................. .................................................. ........................‬ﻣﻼﺣﻈﺎﺕ‪1.4.3‬‬ ‫‪7-1‬‬
‫‪1.5‬‬ ‫‪ ................................................ ..................................................‬ﺍﻻﺳﺘﺨﺪﺍﻡﺍﻟﻤﻘﺼﻮﺩ‬ ‫‪7-1.................‬‬
‫‪1.6‬‬ ‫‪ ............................................... ..................................................‬ﻣﺆﺷﺮﺍﺕﻟﻼﺳﺘﺨﺪﺍﻡ‬ ‫‪7-1.........‬‬
‫‪1.7‬‬ ‫‪................................................. ..................................................‬ﻣﻮﺍﻧﻊ‬ ‫‪8-1...........‬‬
‫‪1.8‬‬ ‫‪ ........................................... ...........................................‬ﺍﻻﺧﺘﺼﺎﺭﺍﺕﻭﺍﻟﺘﻌﺎﺭﻳﻒ‬ ‫‪8-1‬‬
‫‪1.9‬‬ ‫‪ ........................................... ................................................‬ﺍﻟﻮﻇﺎﺉﻒﺍﻟﻤﺴﺘﺨﺪﻣﺔ ﺑﺸﻜﻞ ﻣﺘﻜﺮﺭ‬ ‫‪10-1‬‬
‫‪1.10‬‬ ‫‪ ................................................. .................................................. ...........................‬ﺣﺮﻑﺍﻭ ﺭﻣﺰ‬ ‫ﺩﻟﻴﻞ ‪10-1‬‬
‫ﺍﻟﺒﺪءﺍﻟﺴﺮﻳﻊ ﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ‪1.11 12-1.......... .................................................. ...................‬‬ ‫‪VG70‬‬
‫‪ ................................................ ..................................................‬ﻧﺒﺬﺓﻋﻦ ﺍﻟﻨﻈﺎﻡ ‪2‬‬ ‫‪1-2 ..........‬‬
‫‪ ........................................... ..................................................‬ﻣﻜﻮﻧﺎﺕﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ‪2.1‬‬ ‫‪1-2.‬‬

‫‪ ........................................... .............................................‬ﻣﻜﻮﻧﺎﺕﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ‪2.2‬‬ ‫‪2-2‬‬

‫‪ ........................................... .................................................‬ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‪2.2.1‬‬ ‫‪2 -2‬‬
‫‪ ........................................... ..................................................‬ﺍﻟﻠﻮﺣﺔ ﺍﻟﺠﺎﻧﺒﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‪2.2.2‬‬ ‫‪3-2‬‬
‫‪ ........................................... ..................................................‬ﻭﺣﺪﺓﺍﻟﺘﺤﻜﻢ ﺍﻟﺮﺉﻴﺴﻴﺔ ‪2.3‬‬ ‫‪4-2...........‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ‪2.3.1‬‬ ‫‪4-2...............‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﻠﻮﺣﺔ ﺍﻟﺨﻠﻔﻴﺔ‪2.3.2‬‬ ‫‪5-2................‬‬
‫‪................................................. .................................................. ...............................‬ﻋﺮﺑﺔﺍﻟﺘﺴﻮﻕ ‪2.4‬‬ ‫‪6-2‬‬
‫‪ ................................................. ..................................................‬ﺍﻟﻤﺮﻃﺐ ‪2.5‬‬ ‫‪6-2....................‬‬
‫‪ ........................................... ..................................................‬ﻃﻘﻢﺍﺳﻄﻮﺍﻧﺔ ‪2.6‬‬ ‫‪6-2....................‬‬
‫‪ ................................................. ..................................................‬ﺷﺮﻛﺔ‪2‬ﻭﺣﺪﺓ ‪3‬‬ ‫‪1-3 ...................‬‬
‫‪ .............................................. ................................................‬ﺷﺮﻛﺔ‪2‬ﺍﻻﺳﺘﺨﺪﺍﻡ ﺍﻟﻤﻘﺼﻮﺩ ﻟﻠﻮﺣﺪﺓ ‪3.1‬‬ ‫‪1 -3‬‬
‫‪ .............................................. ..............................................‬ﺷﺮﻛﺔ‪2‬ﻣﻮﺍﺻﻔﺎﺕ ﺍﻟﻮﺣﺪﺓ ‪3.2‬‬ ‫‪1-3‬‬
‫‪ .............................................. ..................................................‬ﻋﺎﻡ‪3.2.1‬‬ ‫‪1-3....................‬‬
‫‪ ........................................... ...........................................‬ﺗﻌﻠﻴﻤﺎﺕﺗﺠﻤﻴﻊ ﺍﻟﻨﻈﺎﻡ ‪3.3‬‬ ‫‪5-3‬‬
‫‪ ........................................... .................................................. ............................‬ﺍﻹﻋﺪﺍﺩ‪3.3.1‬‬ ‫‪5-3‬‬
‫ﻣﻮﺿﻊ ﻣﺴﺒﺎﺭ ‪3.3.27-3 ............................................ ...........................................‬‬ ‫‪IRMA‬‬
‫‪ ........................................... ..................................................‬ﻓﺤﺺﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ ‪3.4‬‬ ‫‪7-3..................‬‬
‫‪ .............................................. ..................................................‬ﺇﺟﺮﺍء ﺍﻟﺘﺼﻔﻴﺮ‪3.4.1‬‬ ‫‪7-3....‬‬
‫‪3.5‬‬ ‫‪ ........................................... ..................................................‬ﺍﻹﻧﺬﺍﺭﺍﺕ‬ ‫‪8-3..........................‬‬
‫‪3.6‬‬ ‫‪................................................. .................................................. ............................‬ﺗﻨﻈﻴﻒ‬ ‫‪8-3‬‬
‫‪3.7‬‬ ‫‪ .............................................. ..................................................‬ﺗﺤﺬﻳﺮﺍﺕ‬ ‫‪8-3...........................‬‬
‫‪3.8‬‬ ‫‪ .............................................. ..................................................‬ﻳﺤﺬﺭ‬ ‫‪10-3.....................‬‬
‫‪ .............................................. .............................................‬ﻣﻌﻠﻮﻣﺎﺕﺍﻟﺼﻴﺎﻧﺔ ‪3.9‬‬ ‫‪10-3‬‬
‫‪................................................. .................................................. ..............................‬ﻳﺜﺒﺖ ‪4‬‬ ‫‪1-4‬‬

‫‪ .............................................. ..................................................‬ﺗﻮﺻﻴﻞﻣﺼﺪﺭ ﺍﻟﻄﺎﻗﺔ ‪4.1‬‬ ‫‪1-4...‬‬

‫ﺍﻟﺨﺎﻣﺲ‬
 ‫‪4.2‬‬ ‫‪ ........................................... ..................................................‬ﺗﻮﺻﻴﻞﻣﺼﺪﺭ ﺍﻟﻐﺎﺯ‬ ‫‪1-4.......‬‬
‫‪4.3‬‬ ‫‪ .............................................. ..................................................‬ﺗﻮﺻﻴﻞﺍﻟﻤﻠﺤﻘﺎﺕ‬ ‫‪2-4......‬‬
‫‪ .......................................... .................................................‬ﺗﻮﺻﻴﻞ ﺩﺍﺉﺮﺓ ﺍﻟﻤﺮﻳﺾ‪4.3.1‬‬ ‫‪2 -4‬‬
‫‪ ........................................... ...........................................‬ﺗﻮﺻﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﺮﻃﻴﺐ (ﺍﺧﺘﻴﺎﺭﻱ)‪4.3.2‬‬ ‫‪3-4‬‬
‫‪ ...........................................‬ﺗﻮﺻﻴﻞ ﺫﺭﺍﻉ ﺗﺤﺪﻳﺪ ﻣﻮﺿﻊ ﺩﺍﺉﺮﺓ ﺍﻟﻤﺮﻳﺾ (ﺍﺧﺘﻴﺎﺭﻱ)‪4.3.3‬‬ ‫‪3-4.........‬‬
‫‪ .............................................. ...........................................‬ﺗﻮﺻﻴﻞ ﺷﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ‪4.3.4‬‬ ‫‪4-4‬‬
‫‪ ........................................... ...........................................‬ﺗﻮﺻﻴﻞ ﻣﺠﻤﻮﻋﺔ ﺍﻷﺳﻄﻮﺍﻧﺎﺕ (ﺍﺧﺘﻴﺎﺭﻱ)‪4.3.5‬‬ ‫‪4-4‬‬
‫‪ ........................................... ..................................................‬ﺍﺧﺘﺒﺎﺭﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ ‪5‬‬ ‫‪1-5 .....................‬‬
‫‪5.1‬‬ ‫‪ .......................................... .............................................‬ﻣﺘﻰﻳﺘﻢ ﺇﺟﺮﺍء ﺍﺧﺘﺒﺎﺭ ﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ‬ ‫‪1-5‬‬
‫‪ ........................................... ..................................................‬ﺇﺟﺮﺍءﺍﺧﺘﺒﺎﺭ ﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ ‪5.2‬‬ ‫‪1-5.....‬‬
‫‪ ........................................... ..................................................‬ﺗﺸﻐﻴﻞﺍﻟﻤﺮﻭﺣﺔ ‪6‬‬ ‫‪1-6......‬‬
‫‪ ................................................ ..................................................‬ﺑﺪء ‪6.1‬‬ ‫‪1-6....................‬‬
‫‪6.2‬‬ ‫‪ ........................................... ..................................................‬ﺗﺨﻄﻴﻂﺍﻟﻮﺍﺟﻬﺔ‬ ‫‪4-6............‬‬
‫‪ .............................................. ............................................‬ﺗﺨﻄﻴﻂ ﻭﺍﺟﻬﺔ ﺍﻻﺳﺘﻌﺪﺍﺩ‪6.2.1‬‬ ‫‪4-6‬‬
‫‪ ........................................... .................................‬ﺗﺨﻄﻴﻂ ﻭﺍﺟﻬﺔ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪6.2.2‬‬ ‫‪8-6‬‬
‫‪6.3‬‬ ‫‪ ........................................... ................................................‬ﺗﺸﻐﻴﻞﺍﻟﺪﻟﻴﻞ ﺍﻟﺮﺉﻴﺴﻲ‬ ‫‪14 -6‬‬
‫‪ .............................................. ..................................................‬ﻭﺿﻊ ﺍﻟﺘﻬﻮﻳﺔ‪6.3.1‬‬ ‫‪14-6....‬‬
‫‪ .............................................. ..................................................‬ﺣﺪﻭﺩ ﺍﻹﻧﺬﺍﺭ‪6.3.2‬‬ ‫‪21-6...........‬‬
‫‪ .............................................. ..................................................‬ﺑﻴﺎﻧﺎﺕ ﺍﻟﻤﺮﺍﻗﺒﺔ‪6.3.3‬‬ ‫‪25-6.....‬‬
‫‪ .............................................. ..................................................‬ﻣﻴﻜﺎﻧﻴﻜﺎ ﺍﻟﺮﺉﺔ‪6.3.4‬‬ ‫‪25-6......‬‬
‫‪ .............................................. .................................................. .............................‬ﺍﻟﺴﺠﻞ‪6.3.5‬‬ ‫‪27-6‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﻨﻈﺎﻡ‪6.3.6‬‬ ‫‪30-6...................‬‬
‫‪6.4‬‬ ‫‪ ........................................... .................................‬ﺗﺸﻐﻴﻞﻣﻔﺎﺗﻴﺢ ﺍﻻﺧﺘﺼﺎﺭ ﺍﻷﺧﺮﻯ‬ ‫‪47-6‬‬
‫‪ .............................................. ..................................................‬ﺗﻌﻠﻴﻖ ﺍﻟﺸﻬﻴﻖ‪6.4.1‬‬ ‫‪48-6......‬‬
‫‪ .............................................. ..................................................‬ﺗﻌﻠﻴﻖ ﺍﻟﺰﻓﻴﺮ‪6.4.2‬‬ ‫‪49-6.......‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺒﺨﺎﺧﺎﺕ‪6.4.3‬‬ ‫‪49-6...............‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺪﻟﻴﻞ‪6.4.4‬‬ ‫‪50-6..................‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺸﻔﻂ‪6.4.5‬‬ ‫‪51-6...................‬‬
‫‪ .............................................. ..................................................‬ﺷﺎﺷﺔ ﺍﻟﻄﺒﺎﻋﺔ‪6.4.6‬‬ ‫‪52-6............‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺘﺠﻤﻴﺪ‪6.4.7‬‬ ‫‪53-6....................‬‬
‫‪ .............................................. ..................................................‬ﻗﻔﻞ ﺍﻟﺸﺎﺷﺔ‪6.4.8‬‬ ‫‪53-6.............‬‬
‫‪ .............................................. ..................................................‬ﺣﺪﻭﺩ ﺍﻹﻧﺬﺍﺭ‪6.4.9‬‬ ‫‪55-6...........‬‬
‫‪6.5‬‬ ‫‪ .............................................. ...........................................‬ﺇﻋﺪﺍﺩﻣﻌﻠﻤﺔ ﺍﻟﺘﻬﻮﻳﺔ‬ ‫‪56-6‬‬
‫‪ ........................................... ..................................................‬ﻗﻢﺑﺈﻳﻘﺎﻑ ﺗﺸﻐﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ‪6.6‬‬ ‫‪58-6...‬‬
‫‪ ........................................... ...........................................‬ﺍﻹﻧﺬﺍﺭﺍﺕﻭﺍﺳﺘﻜﺸﺎﻑ ﺍﻷﺧﻄﺎء ﻭﺇﺻﻼﺣﻬﺎ ‪7‬‬ ‫‪1-7‬‬
‫‪ ........................................... ..................................................‬ﺍﻹﻧﺬﺍﺭﺍﺕ ‪7.1‬‬ ‫‪1-7...........................‬‬
‫‪ .............................................. ..................................................‬ﺟﺪﻭﻝﺭﺳﺎﺉﻞ ﺍﻟﺘﻨﺒﻴﻪ ‪7.2‬‬ ‫‪1-7.....‬‬
‫‪ ........................................... ..................................................‬ﺻﻴﺎﻧﺔﺍﻟﻤﺴﺘﺨﺪﻡ ‪8‬‬ ‫‪1-8 .........‬‬
‫‪8.1‬‬ ‫‪ ........................................... .................................................‬ﺍﻟﺘﻨﻈﻴﻒﻭﺍﻟﺘﻄﻬﻴﺮ‬ ‫‪1- 8‬‬
‫‪ ........................................... ....................‬ﺍﻟﻘﻮﺍﻋﺪ ﺍﻟﻌﺎﻣﺔ ﻟﻠﺘﻨﻈﻴﻒ ﻭﺍﻟﺘﻄﻬﻴﺮ‪8.1.1‬‬ ‫‪1-8‬‬
‫‪ .............................................. ..................................................‬ﺻﻤﺎﻡ ﺍﻟﺰﻓﻴﺮ‪8.1.2‬‬ ‫‪2-8........‬‬
‫ﺇﻋﺎﺩﺓ ﻣﻌﺎﻟﺠﺔ ﺻﻤﺎﻡ ﺍﻟﺰﻓﻴﺮﻭﻓﻘًﺎ ﻟﻠﻤﻮﺍﺻﻔﺔ ‪8.1.32-8.................................‬‬ ‫‪EN ISO 17664‬‬
‫‪ ........................................... ................................‬ﻋﻮﺍﻣﻞ ﺍﻟﺘﻨﻈﻴﻒ ﻭﺍﻟﺘﻄﻬﻴﺮ‪8.1.4‬‬ ‫‪3-8‬‬
‫‪ .............................................. ....................‬ﺗﻨﻈﻴﻒ ﺍﻟﻤﻜﻮﻧﺎﺕ ﻭﺗﻄﻬﻴﺮﻫﺎ‪8.1.5‬‬ ‫‪4-8‬‬

‫‪ ........................................... ..................................................‬ﺍﻻﺧﺘﺒﺎﺭ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ‪8.1.6‬‬ ‫‪6-8.....‬‬

‫ﺍﻟﺴﺎﺩﺱ‬
 ‫‪ ...........................................‬ﺍﻟﻌﻤﺮ ﺍﻻﻓﺘﺮﺍﺿﻲ ﻟﺼﻤﺎﻡ ﺍﻟﺰﻓﻴﺮ‪8.1.7‬‬ ‫‪6-8 ..............................................‬‬
‫ﺻﻤﺎﻡ ﺍﻟﺰﻓﻴﺮ ﺍﻟﻤﻌﺒﺄ‪ :‬ﺍﻟﻌﻤﺮ ﺍﻻﻓﺘﺮﺍﺿﻲ ﻭﻇﺮﻭﻑ ﺍﻟﺘﺨﺰﻳﻦ‪8.1.8‬‬ ‫‪7-8...........................‬‬
‫‪ ................................................ ..................................................‬ﺻﻴﺎﻧﺔﺩﻭﺭﻳﺔ ‪8.2‬‬ ‫‪7-8....‬‬
‫‪ ...........................................................‬ﻣﺒﺎﺩﺉ ﺍﻟﺼﻴﺎﻧﺔ‪8.2.1‬‬ ‫‪7-8 ..............................................‬‬
‫‪ ...........................................‬ﺟﺪﻭﻝ ﺍﻟﺼﻴﺎﻧﺔ ﺍﻟﺪﻭﺭﻳﺔ‪8.2.2‬‬ ‫‪7-8 ..................................‬‬
‫‪ ..............................................‬ﻣﺪﺓ ﺧﺪﻣﺔ ﺍﻟﻤﻨﺘﺞ‪/‬ﺍﻟﻤﻠﺤﻘﺎﺕ‪8.2.3‬‬ ‫‪8-8 ...............................‬‬
‫‪ ...........................................‬ﺍﻟﺼﻴﺎﻧﺔﻓﻲ ﺍﻟﺘﺸﻐﻴﻞ ﻭﺍﻟﻨﻘﻞ ‪8.3‬‬ ‫‪9-8..................‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﻨﻘﻞ‪8.3.1‬‬ ‫‪9-8........‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﺘﺨﺰﻳﻦ‪8.3.2‬‬ ‫‪10-8..................‬‬
‫‪ ...........................................‬ﺍﺳﺘﺒﺪﺍﻝﺍﻟﻤﻮﺍﺩ ﺍﻻﺳﺘﻬﻼﻛﻴﺔ ‪8.4‬‬ ‫‪10-8 ...........................................‬‬
‫‪ .............................................. ..................................................‬ﺍﺳﺘﺒﺪﺍﻝ ﺍﻟﻤﺼﻬﺮ‪8.4.1‬‬ ‫‪10-8..‬‬
‫‪ .............................................. .................................................‬ﺻﻴﺎﻧﺔ ﺍﻟﺒﻄﺎﺭﻳﺔ‪8.4.2‬‬ ‫‪11 -8‬‬
‫‪................................................ ..................................................‬ﻣﺴﺘﺸﻌﺮ ﺍﻷﻛﺴﺠﻴﻦ‪8.4.3‬‬ ‫‪13-8..........‬‬
‫‪ ...........................................‬ﻣﺴﺘﺸﻌﺮ ﺍﻷﻛﺴﺠﻴﻦ ﺍﻟﺒﺎﺭﺍﻣﻐﻨﺎﻃﻴﺴﻲ (ﺍﺧﺘﻴﺎﺭﻱ)‪8.4.4‬‬ ‫‪15-8 ..........................‬‬
‫‪ ...........................................‬ﺍﺳﺘﺒﺪﺍﻝ ﺍﻟﺤﺠﺎﺏ ﺍﻟﺤﺎﺟﺰ‪8.4.5‬‬ ‫‪17-8 ...........................................‬‬
‫‪ ...........................................‬ﺍﺳﺘﺒﺪﺍﻝ ﺍﻟﺤﺠﺎﺏ ﺍﻟﺤﺎﺟﺰ ﻓﻲ ﺍﺗﺠﺎﻩ ﻭﺍﺣﺪ‪8.4.6‬‬ ‫‪18-8..............................‬‬
‫‪ ..............................................‬ﺍﺳﺘﺒﺪﺍﻝ ﺍﻟﻘﻄﻦ ﻟﻤﺮﺷﺢ ﺍﻟﻤﺮﻭﺣﺔ‪8.4.7‬‬ ‫‪19-8 ...................................‬‬
‫‪ ...........................................‬ﻋﻨﺼﺮ ﻣﺮﺷﺢ ﺍﺳﺘﺒﺪﺍﻝ ﻣﺪﺧﻞ ﺍﻟﻐﺎﺯ‪8.4.8‬‬ ‫‪20-8...........................‬‬
‫ﺍﺳﺘﺒﺪﺍﻝ ﺍﻟﻔﻠﺘﺮ (ﺭﻗﻢ ﺍﻟﺠﺰء‪8.4.9130003930( .......................................... :‬‬ ‫‪21-8.......................‬‬
‫‪ ................................................. ..................................................‬ﺗﺼﺮﻑ ‪8.5‬‬ ‫‪21-8...........................‬‬
‫‪................................................. ..................................................‬ﺿﻤﺎﻥ ‪9‬‬ ‫‪1-9...........................‬‬
‫‪................................................. ..................................................‬ﻳﻌﻮﺩ ‪9.1‬‬ ‫‪1-9...........................‬‬
‫‪............................................... ..................................................‬ﻧﻈﺮﻳﺔﺍﻟﺘﺸﻐﻴﻞ ‪10‬‬ ‫‪1-10 .....‬‬
‫‪ ........................................................... ..................................................‬ﺃﻭﺿﺎﻉ ﺍﻟﺘﻬﻮﻳﺔ‪10.1‬‬ ‫‪1-10........‬‬
‫‪ ...........................................‬ﻣﺴﺎﻋﺪﺓ ‪ /‬ﺍﻟﺘﺤﻜﻢ ﻓﻲ ﺍﻟﺘﻬﻮﻳﺔ ‪10.1.1‬‬ ‫ﺍﻟﺘﻬﻮﻳﺔ ‪1-10 ........................................‬‬
‫‪.... ...........................................‬ﺍﻹﻟﺰﺍﻣﻴﺔﺍﻟﻤﺘﻘﻄﻌﺔ ﺍﻟﻤﺘﺰﺍﻣﻨﺔ‪10.1.2‬‬ ‫ﺍﻟﺘﻬﻮﻳﺔ ﺍﻻﺣﺘﻴﺎﻃﻴﺔ ( ﺍﻧﻘﻄﺎﻉ ﺍﻟﺘﻨﻔﺲ ) ‪4-10‬‬
‫‪10.1.3 ................................................. .................‬‬ ‫‪/‬ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﺘﻠﻘﺎﺉﻴﺔ‪5-10‬‬
‫‪10.1.4................................ .................................................. .10-6‬‬ ‫ﺍﻟﺘﻬﻮﻳﺔ ﺛﻨﺎﺉﻴﺔ ﺍﻟﻤﺴﺘﻮﻯ ‪CPAP‬‬
‫)‪10.1.5 ........................................ ........................................... (BIVENT‬‬ ‫ﺿﻐﻂ ﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء ﻏﻴﺮ ‪10-7‬‬
‫‪ .............................................‬ﺍﻟﺠﺮﺍﺣﻲ‪/‬ﺍﻹﻳﺠﺎﺑﻲ ﺍﻟﻤﺴﺘﻤﺮ‪10.1.6‬‬ ‫‪-‬ﻧﻴﻒ ‪8-10‬‬
‫‪................................................................ .................................................. 10-10.................‬ﺕ‪10.1.7‬‬
‫‪10.1.8 .................................................. ........................................... 10-10‬‬ ‫‪NIV-S/T.........................‬‬
‫ﻣﻮﺍﺻﻔﺎﺕﻧﻈﺎﻡ ﺍﻟﺘﻬﻮﻳﺔ ‪11 1-11 ................................ .................................................‬‬ ‫‪VG70‬‬
‫‪ .............................................. ..................................................‬ﺍﻟﻨﻈﺎﻡ‪11.1‬‬ ‫‪1-11 ................................‬‬
‫‪ ........................................................... ..................................................‬ﻋﺎﻡ‪11.1.1‬‬ ‫‪1-11..................‬‬
‫‪ ...........................................................‬ﻇﺮﻭﻑ ﺍﻟﺘﺸﻐﻴﻞ‪11.1.2‬‬ ‫‪2-11 ............................................‬‬
‫‪.................................................‬ﻇﺮﻭﻑ ﻋﺪﻡ ﺍﻟﺘﺸﻐﻴﻞ‪11.1.3‬‬ ‫‪2-11 ...........................................‬‬
‫‪ .............................................. ..................................................‬ﻣﺼﺪﺭ ﺍﻟﻄﺎﻗﺔ‪11.1.4‬‬ ‫ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ‪2-11..........‬‬
‫‪ ........................................ ..................................................‬ﺍﻟﺼﻨﺎﻋﻲ ‪11.2‬‬ ‫‪3-11.................................‬‬
‫‪ ........................................................... ..................................................‬ﻋﺎﻡ‪11.2.1‬‬ ‫‪3-11..................‬‬
‫‪ .............................................. ..................................................‬ﺇﻣﺪﺍﺩ ﺍﻟﻐﺎﺯ‪11.2.2‬‬ ‫‪4-11..............‬‬
‫‪ ...........................................‬ﻣﻮﺻﻼﺕ ﻧﻈﺎﻡ ﺍﻟﻤﺮﻳﺾ‪11.2.3‬‬ ‫‪4-11 ...........................................‬‬
‫‪ .............................................. ..................................................‬ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ‪11.2.4‬‬ ‫‪4-11.........‬‬
‫‪ ..............................................‬ﺍﻟﻄﺎﻗﺔ ﺍﻟﺼﻮﺗﻴﺔ‪11.2.5‬‬ ‫‪..................................................‬‬
‫‪4-11......‬‬

‫‪ ...........................................‬ﺗﻌﻠﻴﻤﺎﺕ ﺍﻷﻣﻦ ﺍﻟﺴﻴﺒﺮﺍﻧﻲ‪11.2.6‬‬ ‫‪4-11 ................................................‬‬

‫ﺳﺎﺑﻌﺎ‬
 ‫‪11.3‬‬ ‫‪ ...........................................‬ﻣﻮﺍﺻﻔﺎﺕﺍﻟﺸﺮﻭﻁ ﺍﻟﻘﻴﺎﺳﻴﺔ‬ ‫ﺍﻟﻘﻨﺎﺓ ‪5-11 ................................‬‬
‫‪11.4‬‬ ‫‪ ............. .................................................. ........................................‬ﺍﻟﻤﻠﻬﻤﺔ‬ ‫ﻗﻨﺎﺓ ‪5-11‬‬
‫‪11.5‬‬ ‫‪ ..... .................................................. .................................................‬ﺍﻟﺰﻓﻴﺮ‬ ‫‪5- 11‬‬
‫‪11.6‬‬ ‫‪ ........................................... ..................................................‬ﺍﻟﻤﺮﺍﻗﺒﺔ‬ ‫‪6-11...................‬‬
‫‪ ........................... .................................................. 7-11..............................................‬ﺍﻹﻧﺬﺍﺭﺍﺕ ‪11.7‬‬
‫‪ ...........................................‬ﺇﻋﺪﺍﺩﺍﺕ ﺍﻟﺘﻨﺒﻴﻪ ﺍﻟﻤﺴﻤﻮﺡ ﺑﻬﺎ‪11.7.1‬‬ ‫‪7-11 .............................................‬‬
‫‪ .............................................. ..............................................‬ﺍﻹﻧﺬﺍﺭﺍﺕ ﺍﻟﻤﺘﻨﻮﻋﺔ‪11.7.2‬‬ ‫‪8-11‬‬
‫‪ ................................................. ..................................................‬ﺍﻟﺘﻬﻮﻳﺔﺃﺳﺎﻟﻴﺐ ‪11.8‬‬ ‫‪8-11......‬‬
‫‪ .............................................. ..............................................‬ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﺨﺎﺿﻌﺔ ﻟﻠﺮﻗﺎﺑﺔ‪11.8.1‬‬ ‫‪8-11‬‬
‫‪ .............................................. ..............................................‬ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﻤﺪﻋﻮﻣﺔ‪11.8.2‬‬ ‫‪8-11‬‬
‫‪ ........................................... ..............................................‬ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﻤﺸﺘﺮﻛﺔ‪11.8.3‬‬ ‫ﺍﻻﺗﺠﺎﻩ ‪9-11‬‬
‫‪ ................................................. ..................................................‬ﻭﻇﻴﻔﺔ‪11.9‬‬ ‫‪9-11...........‬‬
‫‪ .............................................. ..................................................‬ﻭﻇﻴﻔﺔ ﺍﻟﺴﺠﻞ‪11.10‬‬ ‫‪10-11...............‬‬
‫‪ .............................................. ..................................................‬ﻭﻇﺎﺉﻒ ﻣﻔﺘﺎﺡ ﺍﻻﺧﺘﺼﺎﺭ‪11.11‬‬ ‫‪10-11‬‬
‫‪ .............................................. .............................................‬ﺍﻻﺗﺼﺎﻝ‪/‬ﺍﻟﻮﺍﺟﻬﺔ‪11.12‬‬ ‫‪11-11‬‬
‫‪ ........................................... ..................................................‬ﻣﻨﻔﺬ ﺍﺳﺘﺪﻋﺎء ﺍﻟﻤﻤﺮﺿﺔ‪11.12.1‬‬ ‫‪11-11.......‬‬
‫‪ .............................................. ..................................................‬ﻣﻨﻔﺬ ﺇﻳﺜﺮﻧﺖ‪11.12.2‬‬ ‫‪11-11........‬‬
‫ﻣﻨﻔﺬ ‪11.12.312-11............. .................................................. ................................................‬‬ ‫‪RS-232‬‬
‫‪ ........................................... .............................................‬ﻣﻨﻔﺬ ﺇﺧﺮﺍﺝ ﺍﻟﺒﺨﺎﺧﺎﺕ‪11.12.4‬‬ ‫‪12-11‬‬
‫‪ ...........................................‬ﻭﺻﻒ ﺍﻷﻣﻦ ﺍﻟﺴﻴﺒﺮﺍﻧﻲ‪11.12.5‬‬ ‫‪12-11 ........................................‬‬
‫‪................................................ ..................................................‬ﺍﻟﻤﻠﺤﻘﺎﺕ‪11.13‬‬ ‫‪12-11................‬‬
‫ﻣﻌﻠﻤﺎﺕ ﺍﻟﺘﻬﻮﻳﺔ‪ :‬ﺍﻟﻘﻴﻢ ﺍﻻﻓﺘﺮﺍﺿﻴﺔ ﻭﺍﻹﻋﺪﺍﺩﺍﺕ ﺍﻟﻤﺴﻤﻮﺡ ﺑﻬﺎ (ﺍﻟﺘﻜﻮﻳﻦ ﺍﻟﻘﻴﺎﺳﻲ) ‪11.1411-14‬‬
‫‪ ........................................................... ..................................................‬ﺩﻗﺔ ﺍﻟﺘﺴﻠﻴﻢ‪11.15‬‬ ‫ﻣﺨﻄﻂ ‪17-11.......‬‬
‫‪ ........................................... ..................................................‬ﻫﻮﺍﺉﻲ ‪12‬‬ ‫ﺇﺭﺷﺎﺩﺍﺕ ﺍﻟﺘﻮﺍﻓﻖ ‪1-12.....‬‬

‫‪ .......................................... ..................................................‬ﺍﻟﻜﻬﺮﻭﻣﻐﻨﺎﻃﻴﺴﻲ ‪13‬‬ ‫‪1-13...................‬‬

‫ﺛﺎﻣﻨﺎ‬
 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫‪.‬ﻗﻢﺑﻤﺮﺍﺟﻌﺔ ﺟﻤﻴﻊ ﺍﻟﻤﻌﻠﻮﻣﺎﺕ ﺍﻟﻮﺍﺭﺩﺓ ﻓﻲ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞﺟﻴﺪًﺍ ﻗﺒﻞ ﻣﺤﺎﻭﻟﺔ ﺍﺳﺘﺨﺪﺍﻡ ﺍﻟﺠﻬﺎﺯ‬

‫‪.‬ﻭﻳﺠﺐﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﻩ ﺍﻟﻤﻌﺪﺍﺕ ﺗﺤﺖ ﺇﺷﺮﺍﻑ ﺍﻟﻄﺒﻴﺐ‬

‫ﻣﺴﺆﻭﻟﻴﺔ ﺍﻟﺸﺮﻛﺔ ﺍﻟﻤﺼﻨﻌﺔ‪1.1‬‬

‫‪:‬ﺷﺮﻛﺘﻨﺎﻣﺴﺆﻭﻟﺔ ﻋﻦ ﺍﻷﻣﻦ؛ ﻣﻮﺛﻮﻗﻴﺔ ﻭﻭﻇﺎﺉﻒ ﺍﻟﻤﻌﺪﺍﺕ‪ ،‬ﻓﻘﻂ ﻋﻨﺪﻣﺎ ﻳﺘﻢ ﺍﻟﺘﻘﻴﺪ ﺍﻟﺼﺎﺭﻡ ﺑﺎﻟﻤﺘﻄﻠﺒﺎﺕ ﺍﻟﺘﺎﻟﻴﺔ‬

‫‪-‬‬ ‫‪.‬ﻳﺠﻮﺯﻓﻘﻂ ﻟﻸﻓﺮﺍﺩ ﺍﻟﻤﺼﺮﺡ ﻟﻬﻢ ﻣﻦ ﻗﺒﻞ ﺷﺮﻛﺘﻨﺎ ﺇﺟﺮﺍء ﺍﻟﺘﻮﺻﻴﻞ ﻭﺍﻟﺘﻌﺪﻳﻼﺕ ﻭﺍﻹﺻﻼﺣﺎﺕ‬

‫‪-‬‬ ‫ﻳﺠﺐﺃﻥ ﺗﻜﻮﻥ ﺍﻟﻤﻌﺪﺍﺕ ﺍﻟﻜﻬﺮﺑﺎﺉﻴﺔ ﺍﻟﻀﺮﻭﺭﻳﺔ ﻭﺑﻴﺉﺔ ﺍﻟﻌﻤﻞ ﻣﺘﻮﺍﻓﻘﺔ ﻣﻊ ﺍﻟﻤﻌﺎﻳﻴﺮ ﺍﻟﻮﻃﻨﻴﺔ ﻭﺍﻟﻤﻌﺎﻳﻴﺮ ﺍﻟﻤﻬﻨﻴﺔ ﻭﺍﻟﻤﺘﻄﻠﺒﺎﺕﺍﻟﻤﺪﺭﺟﺔ ﻓﻲ ﻫﺬﺍ‬

‫‪.‬ﺍﻟﺪﻟﻴﻞ‬

‫‪.‬ﺳﺘﻘﻮﻡﺷﺮﻛﺘﻨﺎ ﺑﺘﻮﻓﻴﺮ ﻣﻌﻠﻮﻣﺎﺕ ﺍﻟﺨﺪﻣﺔ ﻟﻤﺴﺎﻋﺪﺓ ﺍﻟﻌﻤﻼء‪ ،‬ﺗﺤﺖ ﺇﺷﺮﺍﻑ ﺍﻟﻔﻨﻴﻴﻦ ﺍﻟﻤﺆﻫﻠﻴﻦ‪ ،‬ﻹﺻﻼﺡ ﺍﻟﻤﻌﺪﺍﺕ‬

‫ﻣﺴﺆﻭﻟﻴﺔ ﺍﻟﻤﺸﻐﻞ ﻋﻦ ﺳﻼﻣﺔ ﺍﻟﻤﺮﺿﻰ‪1.2‬‬

‫ﻳﺠﺐﺃﻥ ﻳﺪﺭﻙ ﻣﺸﻐﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻫﺬﺍ ﻣﺴﺆﻭﻟﻴﺘﻪ ﺍﻟﻜﺎﻣﻠﺔ ﻋﻦ ﺍﺧﺘﻴﺎﺭ ﺇﻋﺪﺍﺩﺍﺕ ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﻤﻨﺎﺳﺒﺔ ﻟﻀﻤﺎﻥ ﺍﻟﺘﻬﻮﻳﺔﺍﻟﻤﻨﺎﺳﺒﺔ‬

‫‪.‬ﻭﺳﻼﻣﺔ ﺍﻟﻤﺮﺿﻰ‪ .‬ﺗﻌﺘﻤﺪ ﻣﺴﺆﻭﻟﻴﺔ ﺍﺧﺘﻴﺎﺭ ﺍﻟﻤﺴﺘﻮﻯ ﺍﻟﻤﻨﺎﺳﺐ ﻟﻤﺮﺍﻗﺒﺔ ﺍﻟﻤﺮﻳﺾ ﻋﻠﻰ ﻣﺸﻐﻞ ﺍﻟﺠﻬﺎﺯ ﻓﻘﻂ‬

‫‪.‬ﺟﻤﻴﻊﻣﻌﻠﻮﻣﺎﺕ ﺍﻟﺮﺻﺪ ﻫﻲ ﻟﻺﺷﺎﺭﺓ ﻓﻘﻂ؛ ﻭﻻ ﻳﻨﺒﻐﻲ ﺍﺳﺘﺨﺪﺍﻣﻪ ﻛﺄﺳﺎﺱ ﻭﺣﻴﺪ ﻟﻠﻘﺮﺍﺭﺍﺕ ﺍﻟﻌﻼﺟﻴﺔ ﺃﻭ ﺍﻟﺘﺸﺨﻴﺼﻴﺔ‬

‫ﻋﻨﺪﻣﺎﻳﺘﻢ ﺗﻮﺻﻴﻞ ﺍﻟﻤﺮﻳﺾ ﺑﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ ،‬ﻳﻠﺰﻡ ﺍﻻﻫﺘﻤﺎﻡ ﺍﻟﻤﺴﺘﻤﺮ ﻣﻦ ﻗﺒﻞ ﺃﻓﺮﺍﺩ ﻃﺒﻴﻴﻦ ﻣﺆﻫﻠﻴﻦ ﻣﻦ ﺃﺟﻞ ﺍﺗﺨﺎﺫﺇﺟﺮﺍء ﺗﺼﺤﻴﺤﻲ‬

‫‪.‬ﻓﻮﺭﻱ ﻓﻲ ﺣﺎﻟﺔ ﺣﺪﻭﺙ ﺧﻠﻞ ﻭ‪/‬ﺃﻭ ﺣﺪﻭﺙ ﺇﻧﺬﺍﺭ‬

‫ﺳﺘﻮﻓﺮﺍﻟﺸﺮﻛﺔﺭﺳﻤًﺎﺗﺨﻄﻴﻄﻴًﺎﻭﻇﻴﻔﻴًﺎﺑﻨﺎءً ﻋﻠﻰ ﻃﻠﺐ ﺍﻟﻤﺴﺘﺨﺪﻡ ﻣﻘﺎﺑﻞ ﺭﺳﻮﻡ‪،‬ﻣﺼﺤﻮﺑًﺎ ﺑﺸﺮﺡ ﺣﻮﻝ ﻃﺮﻳﻘﺔ ﺍﻟﻤﻌﺎﻳﺮﺓ ﻭﻣﻌﻠﻮﻣﺎﺕﺃﺧﺮﻯ‪ ،‬ﻭﺫﻟﻚ‬

‫ﻟﻤﺴﺎﻋﺪﺓ ﺍﻟﻤﺴﺘﺨﺪﻣﻴﻦ ﻋﻠﻰ ﺍﻟﺴﻤﺎﺡ ﻟﻠﻤﻮﻇﻔﻴﻦ ﺍﻟﻔﻨﻴﻴﻦ ﺍﻟﻤﻨﺎﺳﺒﻴﻦ ﺑﺈﺻﻼﺡ ﺟﺰء ﺍﻟﻤﻌﺪﺍﺕ ﺍﻟﺬﻱﻳﺴﻤﺢ ﻟﻠﻤﺴﺘﺨﺪﻡ ﺑﺼﻴﺎﻧﺘﻪ ﻋﻠﻰ ﺍﻟﻨﺤﻮ‬

‫‪.‬ﺍﻟﻤﻨﺼﻮﺹ ﻋﻠﻴﻪ‬

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 ‫ﺍﻟﺘﻌﺎﺭﻳﻒ‪1.3‬‬

‫‪:‬ﻳﺴﺘﺨﺪﻡﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ ﺛﻼﺛﺔ ﻣﺆﺷﺮﺍﺕ ﺧﺎﺻﺔ ﻟﻨﻘﻞ ﻣﻌﻠﻮﻣﺎﺕ ﺫﺍﺕ ﻃﺒﻴﻌﺔ ﻣﺤﺪﺩﺓ‪.‬ﻳﺸﻤﻠﻮﺍ‬

‫ﺍﻟﻤﺮﻳﺾﺃﻭ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‬

‫‪.‬ﻣﻌﺪﺍﺕ‬

‫ﺍﻟﺘﻲﺗﺠﻌﻞ ﻋﻤﻠﻴﺔ‬

‫ﺍﻟﺘﺤﺬﻳﺮﺍﺕ ﻭﺍﻟﺘﻨﺒﻴﻬﺎﺕ ﻭﺍﻟﻤﻼﺣﻈﺎﺕ‪1.4‬‬

‫ﺍﻟﺘﺤﺬﻳﺮﺍﺕ‪1.4.1‬‬

‫ﻭﻓﻬﻢﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ‬
‫‪:‬ﻣﺸﺘﻤﻞ‬

‫‪-‬‬ ‫ﺟﻤﻴﻊﺗﻮﺻﻴﻼﺕ ﺍﻟﻨﻈﺎﻡ ﺟﻤﻴﻊ‬

‫‪-‬‬ ‫ﺍﻟﺘﺤﺬﻳﺮﺍﺕﻭﺍﻟﺘﺤﺬﻳﺮﺍﺕ‬
‫‪-‬‬ ‫ﺇﺟﺮﺍءﺍﺕﺍﻟﺘﺸﻐﻴﻞ ﻟﻜﻞ ﻣﻜﻮﻥ ﻣﻦ ﻣﻜﻮﻧﺎﺕ ﺍﻟﻨﻈﺎﻡ‬
‫ﺗﻴﻢ‬

‫ﺍﺳﺘﺨﺪﺍﻡﺍﻟﺘﻔﺘﻴﺶ ﻭﻓﻘﺎ ﻝ‬
‫ﺍﻟﻔﺼﻞﺍﻟﺨﺎﻣﺲ ﻣﻦ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ‪ ،‬ﻭﻻ ﺗﺴﺘﺨﺪﻣﻪ ﺇﻻ ﺑﻌﺪ ﺍﻟﺘﺄﻛﺪ ﻣﻦ ﺃﻥ ﺍﻟﻮﻇﻴﻔﺔ ﻃﺒﻴﻌﻴﺔ‪ .‬ﻳﺘﺤﻤﻞ ﺍﻟﻤﺴﺘﺨﺪﻡ ﻣﺴﺆﻭﻟﻴﺔ ﻋﻮﺍﻗﺐﺍﺳﺘﺨﺪﺍﻡ ﺍﻟﻮﻇﻴﻔﺔ‬

‫‪.‬ﺩﻭﻥ ﺇﺟﺮﺍء ﺗﺄﻛﻴﺪ ﺍﻟﻮﻇﻴﻔﺔ‬

‫ﺹﻳﺤﺘﺎﺝ ﺇﻟﻰ ﺷﺎﻣﻠﺔ‬

‫ﻣﻦﻗﺒﻞ ﺍﻟﻤﻌﺘﻤﺪﻳﻦ ﻭﺍﻟﻤﺪﺭﺑﻴﻦ‬

‫ﺍﻧﻪﺗﺸﻐﻴﻞ ﻭﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﺍ‬

‫‪.‬ﺍﻟﺠﻬﺎﺯﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ ﺍﻟﺴﺮﻳﺮﻱ ﺍﻷﻭﻝ ﻣﻊ ﺍﻟﻤﺮﻳﺾ‬

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 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﺇﻣﻜﺎﻧﻴﺔﺍﻹﺻﺎﺑﺔ ﺍﻟﺠﺴﺪﻳﺔ ﻓﻘﻂ‬

‫ﻳﺠﺐﺃﻥ ﻳﺤﺎﻭﻝ ﺍﻟﻤﻮﻇﻔﻮﻥ ﺍﻟﻤﺆﻫﻠﻮﻥ ﺻﻴﺎﻧﺔ ﺃﻭ ﺇﺟﺮﺍء ﺗﻌﺪﻳﻼﺕ ﻣﻌﺘﻤﺪﺓ ﻋﻠﻴﻬﺎ‬

‫ﻗﻢﺑﺘﻮﺻﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻭﺗﺸﻐﻴﻠﻪ‬

‫ﺷﺮﻛﺘﻨﺎ'ﺱﺍﺗﺼﺎﻝﺍﻹﺟﺮﺍء‪ ،‬ﻭﺍﻟﺬﻱ ﻳﺘﻀﻤﻦ ﻣﻌﺎﻳﺮﺓ ﺍﻟﻨﻈﺎﻡ ﺍﻟﻤﺨﺘﻠﻔﺔ‬

‫ﻭﻇﺎﺉﻒﺩﻋﻢ ﺍﻟﺤﻴﺎﺓ ﻻ‬
‫ﻟﻔﺘﺮﺓﺃﻃﻮﻝﺿﻤﺎﻧًﺎ‪ :‬ﺍﺑﺪﺃ ﺍﻟﺘﻬﻮﻳﺔ ﺑﺎﺳﺘﺨﺪﺍﻡ ﺟﻬﺎﺯ ﺗﻬﻮﻳﺔ ﻣﺴﺘﻘﻞ (ﺣﻘﻴﺒﺔ ﺍﻹﻧﻌﺎﺵ)‬
‫‪.‬ﺫﻳﺎ‪2‬ﺗﺮﻛﻴﺰ‬

‫ﺗﺄﻛﺪﻣﻦ ﺍﻟﺘﺤﻘﻖ ﻣﻦ ﺍﻟﻤﻌﺪﺍﺕ‬

‫‪،‬ﻛﻤﺎ ﻫﻮ ﻣﻮﺿﺢ ﻓﻲ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ )ﺍﺧﺘﺒﺎﺭ ﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ( ‪ PUT‬ﻟﻠﺘﺸﻐﻴﻞﺍﻟﺴﻠﻴﻢ‪ ،‬ﻭﺇﺫﺍ ﻛﺎﻥ ﺫﻟﻚﻣﻨﺎﺳﺒًﺎ‪ ،‬ﻗﻢ ﺑﺘﺸﻐﻴﻞ‬

‫ﺟﻬﺎﺯﻣﺮﺍﻗﺒﺔ ﻣﺘﻜﺮﺭ‬
‫ﻭﻻﻳﻘﻮﻡ ﺑﺘﻔﻌﻴﻞ ﺍﻹﻧﺬﺍﺭﺍﺕ ﻟﺠﻤﻴﻊ ﺃﻧﻮﺍﻉ ﺍﻟﺤﺎﻻﺕ ﺍﻟﺨﻄﻴﺮﺓ ﻟﻠﻤﺮﺿﻰ ﺍﻟﻤﻮﺟﻮﺩﻳﻦ ﻋﻠﻰ ﺃﺟﻬﺰﺓ ﺩﻋﻢ ﺍﻟﺤﻴﺎﺓ‬

‫ﻣﺮﺍﻗﺒﺘﻬﺎﺑﺸﻜﻞ ﻣﻨﺎﺳﺐ ﻓﻲ ﺟﻤﻴﻊ‬

‫‪.‬ﺍﻷﻭﻗﺎﺕ‬

‫‪,‬ﻣﻌﺪﺍﺕﺍﻟﺘﻨﻔﺲ ﺍﻟﻴﺪﻭﻳﺔ‬

‫‪.‬ﻕﺇﻟﻰ ﻣﻨﻔﺬ ﺍﻟﻌﺎﺩﻡ‬

‫ﺗﺮﺗﺒﻂﺑﺎﻟﺼﺤﻴﺢ‬

‫ﻣﻠﻮﺛﺔﺑﺴﻮﺍﺉﻞ ﺍﻟﺠﺴﻢ ﺃﻭ‬

‫ﺍﻟﻐﺎﺯﺍﺕﻣﻨﺘﻬﻴﺔ ﺍﻟﺼﻼﺣﻴﺔ ﺃﺛﻨﺎء ﺍﻻﺳﺘﺨﺪﺍﻡ ﺍﻟﻌﺎﺩﻱ‪ ،‬ﻭﻗﺪ ﻳﺼﺒﺢ ﻣﺴﺎﺭ ﺍﻟﻐﺎﺯ ﺍﻟﺸﻬﻴﻖﻣﻠﻮﺛًﺎ‬
‫‪.‬ﺃﻳﻮﻥ‬

‫ﺳﻴﺪ‪.‬ﺇﻋﺎﺩﺓ ﺍﻻﺳﺘﺨﺪﺍﻡ ﻟﻼﺳﺘﺨﺪﺍﻡ ﺍﻟﻔﺮﺩﻱ‬

‫‪.‬ﻳﻤﻜﻦﺃﻥ ﺗﺴﺒﺐ ﺍﻟﺨﺮﺍﻃﻴﻢ ﻋﺪﻭﻯ ﻣﺘﺼﺎﻟﺒﺔ‬

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 ‫ﻩﺍﻟﻤﻘﺎﻭﻣﺔ ﻭﺍﻻﻣﺘﺜﺎﻝ‬

‫ﻭﺣﺪﺓﺍﻟﺘﺤﻜﻢ ﻭﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‬

‫ﻧﻴﻮﻳﻮﺭﻙﻣﻜﺎﻓﺤﺔ ﺳﺎﻛﻨﺔ ﺃﻭ ﻛﻬﺮﺑﺎﺉﻴﺎ‬

‫ﺃﻭﺍﻟﺘﺠﻤﻌﺎﺕ ﺍﻟﻔﺮﻋﻴﺔ ﻝ‬
‫ﻳﻤﻜﻦﻟﻨﻈﺎﻡ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﺗﻐﻴﻴﺮ ﺗﺪﺭﺝ ﺍﻟﻀﻐﻂ ﻋﺒﺮ ﻧﻈﺎﻡ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻭﺃﻥ ﻣﺜﻞ ﻫﺬﻩ ﺍﻟﺘﻐﻴﻴﺮﺍﺕ ﻓﻲ ﻧﻈﺎﻡ ﺍﻟﺘﻨﻔﺲﺍﻟﺼﻨﺎﻋﻲ ﻳﻤﻜﻦ‬

‫ﺃﻥ ﺗﺆﺛﺮ ﻋﻠﻰ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‬

‫‪.‬ﺣﺮﻭﻕﺑﺎﻃﻠﺔ‬

‫‪.‬ﻣﻜﻮﻧﺎﺕﻟﻮ‬

‫ﺧﺰﺍﻧﺎﺕﺍﻟﻤﻴﺎﻩ ﺍﻟﻤﺮﻃﺒﺔ) ﻋﻠﻰ‬

‫ﺃﻋﻠﻰﺃﻭ ﻓﻮﻕ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ .‬ﻗﺪ ﺗﺆﺩﻱ ﺍﻟﺴﻮﺍﺉﻞ ﺍﻟﺘﻲ ﺗﺪﺧﻞ ﺇﻟﻰ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﺇﻟﻰ ﺣﺪﻭﺙ ﺧﻠﻞ ﻓﻲ ﺍﻟﻤﻌﺪﺍﺕ‬

‫ﻳﺠﺐﺃﻥ ﺗﻜﻮﻥ ﻣﺘﺼﻼ ﻓﻘﻂ ﺏ‬

‫‪.‬ﺇﻣﺪﺍﺩﺍﺕﺍﻟﺘﻴﺎﺭ ﺍﻟﻜﻬﺮﺑﺎﺉﻲ ﻣﻊ ﺍﻷﺭﺽ ﺍﻟﻮﺍﻗﻴﺔ‬

‫ﺍﻟﺘﺤﺬﻳﺮﺍﺕ‪1.4.2‬‬

‫ﻛﻠﻤﺎﺍﺭﺗﻔﻌﺖ ﺍﻟﻘﻮﻯ ﻭ‬

‫ﻣﺤﺎﻭﻟﺔﺍﺳﺘﻜﺸﺎﻑ ﺍﻷﺧﻄﺎء ﻭﺇﺻﻼﺣﻬﺎ ﻭ‬

‫ﺇﺻﻼﺡﺍﻟﻔﺸﻞ‪ .‬ﺇﺫﺍ ﻟﻢ ﺗﺘﻤﻜﻦ ﻣﻦ ﺇﺻﻼﺡ ﺍﻟﺠﻬﺎﺯ‪ ،‬ﻓﺎﻃﻠﺐ ﻣﻦ ﻣﻤﺜﻞ ﺍﻟﺨﺪﻣﺔ ﺍﻟﻤﻌﺘﻤﺪ ﺍﻟﻘﻴﺎﻡ ﺑﺬﻟﻚ‬

‫ﻓﻲﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ؛ ﻻ ﺗﺴﺘﺨﺪﻡ ﺇﺫﺍ‬

‫‪.‬ﻣﻌﻴﺐ‪.‬ﺍﺳﺘﺒﺪﻝ ﻋﻠﻰ ﺍﻟﻔﻮﺭ ﺍﻷﺟﺰﺍء ﺍﻟﻤﻜﺴﻮﺭﺓ ﺃﻭ ﺍﻟﻤﻔﻘﻮﺩﺓ ﺃﻭ ﺍﻟﺒﺎﻟﻴﺔ ﺃﻭ ﺍﻟﻤﺸﻮﻫﺔ ﺃﻭ ﺍﻟﻤﻠﻮﺛﺔ‬

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 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫‪ .nt‬ﺍﻛﺘﻤﻞﺇﻋﺪﺍﺩ‬

‫ﺍﻻﺗﺼﺎﻻﺕﺍﻹﻟﻜﺘﺮﻭﻧﻴﺔ ﻭﺍﻟﺘﺮﺩﺩﺍﺕ ﺍﻟﻼﺳﻠﻜﻴﺔ‬

‫ﺍﻟﻤﺘﻬﺎﻟﻜﺔ‪،‬ﺃﻭ ﺍﻟﻤﻠﻮﺛﺔ ﺑﻬﺎ‬

‫ﺍﻟﻤﻮﺍﺩﺍﻟﻘﺎﺑﻠﺔ ﻟﻼﺷﺘﻌﺎﻝ ﻣﺜﻞ ﺍﻟﺸﺤﻮﻡ ﺃﻭ ﺍﻟﺰﻳﻮﺕ‪ .‬ﻳﻤﻜﻦ ﺑﺴﻬﻮﻟﺔ ﺍﻟﻮﺻﻮﻝ ﺇﻟﻰ ﺍﻟﻤﻨﺴﻮﺟﺎﺕ ﻭﺍﻟﺰﻳﻮﺕ ﻭﺍﻟﻤﻮﺍﺩ ﺍﻟﻘﺎﺑﻠﺔ ﻟﻼﺣﺘﺮﺍﻕ ﺍﻷﺧﺮﻯ‬

‫ﺇﻳﻨﺲﻟﻠﺘﻌﺎﻣﻞ ﻣﻊ ﺍﻟﻤﻌﺪﻳﺔ‬
‫ﻣﺎﺩﺓ‪.‬ﺗﺪﺭﻙ ﺷﺮﻛﺘﻨﺎ ﺃﻥ ﻣﻤﺎﺭﺳﺎﺕ ﺍﻟﺘﻨﻈﻴﻒ ﻭﺍﻟﺘﻌﻘﻴﻢ ﻭﺍﻟﺼﺮﻑ ﺍﻟﺼﺤﻲ ﻭﺍﻟﺘﻄﻬﻴﺮ ﺗﺨﺘﻠﻒ ﺑﺸﻜﻞ ﻛﺒﻴﺮ ﺑﻴﻦ ﻣﺆﺳﺴﺎﺕ ﺍﻟﺮﻋﺎﻳﺔﺍﻟﺼﺤﻴﺔ‪ .‬ﻻ‬

‫ﻳﻤﻜﻦ ﻟﺸﺮﻛﺘﻨﺎ ﺃﻥ ﺗﺤﺪﺩ ﺃﻭ ﺗﻄﻠﺐ ﻣﻤﺎﺭﺳﺎﺕ ﻣﺤﺪﺩﺓ ﺗﻠﺒﻲ ﺟﻤﻴﻊ ﺍﻻﺣﺘﻴﺎﺟﺎﺕ‪ ،‬ﺃﻭ ﺃﻥ ﺗﻜﻮﻥ ﻣﺴﺆﻭﻟﺔ ﻋﻦﻓﻌﺎﻟﻴﺔ ﺍﻟﺘﻨﻈﻴﻒ ﻭﺍﻟﺘﻌﻘﻴﻢ ﻭﻏﻴﺮﻫﺎ ﻣﻦ‬

‫ﺍﻟﻤﻤﺎﺭﺳﺎﺕ ﺍﻟﺘﻲ ﺗﺘﻢ ﻓﻲ ﺭﻋﺎﻳﺔ ﺍﻟﻤﺮﺿﻰ‬

‫ﻩﻣﻦ ﻣﺨﺪﺭ ﻗﺎﺑﻞ ﻟﻼﺷﺘﻌﺎﻝ‬

‫ﺗﺄﻛﺪﻣﻦ ﺗﻮﺻﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‬

‫ﻗﻢﺑﺈﺯﺍﻟﺔ ﻛﻞ ﺍﻟﻄﺎﻗﺔ ﻋﻦ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻋﻦ ﻃﺮﻳﻖ ﻓﺼﻞ ﻣﺼﺪﺭ ﺍﻟﻄﺎﻗﺔ ﻭﺇﻳﻘﺎﻑ ﺗﺸﻐﻴﻠﻪ ﺑﺎﻟﻜﺎﻣﻞ‬

‫ﺇﺩﺍﻟﺴﺠﺎﺉﺮ‪ ،‬ﻭﺟﻤﻴﻊ ﻏﻴﺮﻫﺎ‬

‫ﻣﺼﺎﺩﺭﺍﻻﺷﺘﻌﺎﻝ (ﻋﻠﻰ ﺳﺒﻴﻞ ﺍﻟﻤﺜﺎﻝ‪ ،‬ﺃﺩﻭﻳﺔ ﺍﻟﺘﺨﺪﻳﺮ ﺍﻟﻘﺎﺑﻠﺔ ﻟﻼﺷﺘﻌﺎﻝ ﻭ‪/‬ﺃﻭ ﺍﻟﺴﺨﺎﻧﺎﺕﺑﻌﻴﺪًﺍ) ﻋﻦ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻭ‬

‫ﻳﺘﻢﺗﻮﺻﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻣﻦ‬

‫ﺃﻭﻣﻨﻔﺬ ﺍﻟﻌﺎﺩﻡ ﺃﻭ ﻣﺪﺧﻞ ﺍﻟﻬﻮﺍء ﺃﻭ‬

‫‪.‬ﺭ‬

‫‪.‬ﻏﺮﻓﺔﺝ‬

‫‪.‬ﻣﺨﺎﻟﻴﻂﻣﻊ ﺍﻟﻬﻴﻠﻴﻮﻡ‬

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‫ﺟﻬﺎﺯﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻣﺜﺒﺖ ﻋﻠﻰ ﻋﺮﺑﺔ ﺍﻟﺘﺴﻮﻕ‬

‫ﺗﻌﻤﻞ ﺑﺎﻟﻠﻤﺲ ﺃﻭ ‪ LCD‬ﻋﻠﻰﺷﺎﺷﺔ‬

‫ﻭﻫﻮﺍﻟﻨﻈﺎﻡ ﻓﻲ ﺍﻟﺨﺪﻣﺔ‬

‫‪.‬ﺧﺪﻣﺔﺯﻳﺪ ﻓﻘﻂ‬

‫ﻟﻦﺃﻛﻮﻥ ﻓﻲ ﺍﻟﺨﺪﻣﺔ ﻷﻛﺜﺮ ﻣﻦ ﺫﻟﻚ‬

‫‪.‬ﺍﻟﺮﺣﻴﻖﻓﻲ ﺃﻱ ﻧﻮﻉ ﻣﻦ ﺍﻟﺴﻮﺍﺉﻞ‬

‫ﺟﺎﻧﺐﺍﻟﺘﺸﻐﻴﻞ ﺍﻟﻤﺤﺪﺩ‬

‫‪ %.‬ﻧﺴﺒﺔﺍﻟﺮﻃﻮﺑﺔ ﺍﻟﻨﺴﺒﻴﺔ‬

‫‪.‬ﺭﻃﻮﺑﺔ ﻧﺴﺒﻴﺔ ~‪95%‬‬

‫‪.‬ﺟﺰءﻣﻦ ﺍﻟﻨﻈﺎﻡ‬

‫ﻣﺮﻃﺐﺇﺩ؛ ﻻ ﺗﻘﻢ ﺑﺘﻮﺻﻴﻞ‬

‫ﺗﺤﻘﻖﺑﻌﻨﺎﻳﺔ ﻣﻦ ﻣﺼﻴﺪﺓ ﺍﻟﻤﻴﺎﻩ ﻭ‬

‫ﺍﺑﺤﺚﻋﻦ ﺍﻟﻤﺎء ﻓﻲ ﺍﻟﺨﺮﻃﻮﻡ‪ .‬ﺇﺫﺍ ﺗﻢ ﺍﻟﻌﺜﻮﺭ ﻋﻠﻰ ﺍﻟﻤﺎء ﻓﻲ ﺍﻟﺨﺮﻃﻮﻡ‪ ،‬ﻓﻴﺠﺐ ﺇﺯﺍﻟﺔ ﻫﺬﺍ ﺍﻟﻤﺎء‪ .‬ﻛﻤﺎ ﺃﻧﻪ‬
‫‪ wer‬ﻣﻦﺃﻧﺎﺑﻴﺐ ﺍﻟﻤﺮﻳﺾ‪.‬‬

‫ﻳﺆﺩﻱ ﺑﺸﻜﻞ ﻓﻌﺎﻝ ﺇﻟﻰ ‪y‬ﻣﻨﻔﺬ‬

‫ﻟﻤﺘﻄﻠﺒﺎﺕ ‪ ME‬ﺇﻧﺸﺎءﻧﻈﺎﻡ ﻣﻌﺪﺍﺕ ﻃﺒﻴﺔ‪ ،‬ﻭﻳﻤﻜﻦ ﺃﻥ ﻳﺆﺩﻱ ﺇﻟﻰ ﺍﻧﺨﻔﺎﺽ ﻣﺴﺘﻮﻯ ﺍﻟﺴﻼﻣﺔ‪ ،‬ﺗﺄﻛﺪ ﻣﻦ ﺍﻣﺘﺜﺎﻝ ﻧﻈﺎﻡ‬
‫ﻳﻜﻮﻥ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺬﻱ ﻳﺘﺼﻞﻣﺴﺆﻭﻻً ﻋﻦ ﻣﻌﻴﺎﺭ ﺍﻟﻤﺘﻄﻠﺒﺎﺕ ﺍﻟﻤﻄﺒﻘﺔ ﻋﻠﻰ ﻧﻈﺎﻡ ﺍﻟﻤﻌﺪﺍﺕ ‪.IEC60601-1:2005‬‬
‫‪.‬ﺍﻟﻄﺒﻴﺔ‬

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 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﻣﻼﺣﻈﺎﺕ‪1.4.3‬‬

‫ﺇﻣﻜﺎﻧﻴﺔﺍﺳﺘﺨﺪﺍﻡ ﺃﻱ ﺟﻬﺎﺯ ﺗﻬﻮﻳﺔ‬

‫ﻋﻄﻞﺑﺴﺒﺐ ﺍﻟﺘﺸﻐﻴﻞ ﺃﻭ ﺍﻟﺼﻴﺎﻧﺔ ﺍﻟﺘﻲ ﻳﻘﻮﻡ ﺑﻬﺎ ﺃﻱ ﺷﺨﺺ ﻏﻴﺮ ﻣﺪﺭﺏ ﻟﺪﻳﻨﺎ‬

‫ﻣﻘﺎﻭﻣﺔﺍﻟﻤﺮﻳﺾ‬

‫ﻳﻤﻜﻦﺃﻥ ﺗﺨﺘﻠﻒ ﺣﺎﻟﺔ ﺍﻟﻤﺮﻳﺾ‬

‫ﻣﺤﻮﻝﻓﻲ ﺃﻱ ﺳﻮﺍﺉﻞ‪ .‬ﻳﺮﻯ‬

‫ﻟﻼﺳﺘﺨﺪﺍﻡﺩﺍﺧﻞ ﺍﻟﻤﺮﻳﺾ‬

‫ﻳﺘﻢﺍﻟﺘﻌﺒﻴﺮ ﻋﻦ ﻫﺬﺍ ﺍﻟﺪﻟﻴﻞ‬

‫ﺑﺎﺳﺘﺜﻨﺎء ﺍﻟﺤﺎﻻﺕ ﺍﻟﻤﺤﺪﺩﺓ ﻣﻊ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺃﺧﺮﻯ ‪)،‬ﺩﺭﺟﺔ ﺍﻟﺤﺮﺍﺭﺓ ﺍﻟﻘﻴﺎﺳﻴﺔ ﻭﺍﻟﻀﻐﻂ ﺍﻟﺠﺎﻑ( ‪ STPD‬ﻋﻨﺪﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ‬

‫ﻓﻲ ‪ "st 3008‬ﻣﻌﻠﻮﻣﺎﺕﺍﻟﺤﺪﺙ‬

‫‪.‬ﻧﺎﻧﻮﻏﺮﺍﻡ‬

‫ﺍﻻﺳﺘﺨﺪﺍﻡ ﺍﻟﻤﻘﺼﻮﺩ‪1.5‬‬

‫ﺇﻟﻰ ﺗﻮﻓﻴﺮ ﻋﻼﺝ ﺗﻬﻮﻳﺔ ﻣﺴﺘﻤﺮ ﻟﻠﻤﺮﺿﻰ ﻭﻣﺮﺍﻗﺒﺔ ﺍﻟﻤﺮﺿﻰ ﺍﻟﺬﻳﻦ ﻳﻌﺎﻧﻮﻥ ﻣﻦ ﻓﺸﻞ ﺍﻟﺠﻬﺎﺯﺍﻟﺘﻨﻔﺴﻲ ﺃﻭ ‪ VG70‬ﻳﻬﺪﻑﻧﻈﺎﻡ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‬

‫‪.‬ﻗﺼﻮﺭ ﺍﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺴﻲ‪ ،‬ﻭﺍﻟﺬﻳﻦ ﻳﺤﺘﺎﺟﻮﻥ ﺇﻟﻰ ﺩﻋﻢ ﺍﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺴﻲ‬

‫ﻣﺆﺷﺮﺍﺕ ﻟﻼﺳﺘﺨﺪﺍﻡ‪1.6‬‬

‫ﻋﺒﺎﺭﺓ ﻋﻦ ﺟﻬﺎﺯ ﻳﺘﻢ ﺍﻟﺘﺤﻜﻢ ﻓﻴﻪﺇﻟﻜﺘﺮﻭﻧﻴًﺎ ﻭﻳﻌﻤﻞ ﺑﺎﻟﻄﺎﻗﺔ ﺍﻹﻟﻜﺘﺮﻭﻧﻴﺔ‪ ،‬ﻭﻳﺴﺘﺨﺪﻡﻓﻲ ‪ VG70‬ﺟﻬﺎﺯﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻠﺮﻋﺎﻳﺔ ﺍﻟﺤﺮﺟﺔ‬

‫ﻭﺣﺪﺓ ﺍﻟﻌﻨﺎﻳﺔ ﺍﻟﻤﺮﻛﺰﺓ ﻟﻠﺮﻋﺎﻳﺔ ﺍﻟﺤﺮﺟﺔ ﺃﻭ ﻓﻲ ﻗﺴﻢ ﺍﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺴﻲ ﺃﻭﻗﺴﻢ ﺍﻟﻄﻮﺍﺭﺉﻹﻧﻘﺎﺫ ﻭﻋﻼﺝ ﻣﺮﻳﺾ ﺍﻟﻘﺼﻮﺭﺍﻟﺘﻨﻔﺴﻲ‪ ،‬ﻭﻓﻲ ﺃﻗﺴﺎﻡ‬

‫‪.‬ﺃﺧﺮﻯ ﻟﺘﻘﺪﻳﻢ ﺍﻟﺪﻋﻢ ﺍﻟﺘﻨﻔﺴﻲ ﻟﻠﻤﺮﻳﺾ‬

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 ‫‪:‬ﻳﺠﺐﺍﺳﺘﺨﺪﺍﻡ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻠﻌﻨﺎﻳﺔ ﺍﻟﻤﺮﻛﺰﺓ ﻓﻘﻂ ﻣﻦ ﻗﺒﻞ‬

‫•‬ ‫‪.‬ﻣﻘﺪﻣﻮ ﺍﻟﺮﻋﺎﻳﺔ ﺍﻟﺼﺤﻴﺔ ﺍﻟﻤﻬﻨﻴﺔ‬

‫•‬ ‫‪.‬ﺍﻟﻔﻨﻴﻴﻦ ﺍﻟﺬﻳﻦ ﺗﻠﻘﻮﺍ ﺍﻟﺘﺪﺭﻳﺐ ﻋﻠﻰ ﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﺍ ﺍﻟﻨﻈﺎﻡ‬

‫ﻳﻨﻄﺒﻖﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻠﺮﻋﺎﻳﺔ ﺍﻟﺤﺮﺟﺔ ﻋﻠﻰ ﺍﻟﻤﺮﻳﺾ ﺍﻟﺬﻱ ﻳﺒﻠﻎ ﻭﺯﻧﻪ ‪ 3‬ﻛﺠﻢ ‪ )7‬ﺃﺭﻃﺎﻝ) ﻋﻠﻰ ﺍﻷﻗﻞ‪ ،‬ﻭﻳﺤﺘﺎﺝ ﺇﻟﻰ ﺍﻷﻧﻮﺍﻉﺍﻟﺘﺎﻟﻴﺔ ﻣﻦ‬
‫ﺃﻭ )ﺃﻭ ﺃﻧﺒﻮﺏﺑﻀﻊ ﺍﻟﻘﺼﺒﺔ ﺍﻟﻬﻮﺍﺉﻴﺔ ‪ ET‬ﺑﻮﺍﺳﻄﺔ( ﺩﻋﻢ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ :‬ﺍﻟﺘﻬﻮﻳﺔ ﺑﺎﻟﻀﻐﻂ ﺍﻹﻳﺠﺎﺑﻲ‪ ،‬ﺍﻟﺘﻲ ﻳﺘﻢ ﺗﻮﺻﻴﻠﻬﺎ ﺑﻄﺮﻳﻘﺔ ﺟﺮﺍﺣﻴﺔ‬
‫‪.‬ﻭﻏﻴﺮﻫﺎ ﻣﻦ ﺃﻭﺿﺎﻉﺍﻟﺘﻬﻮﻳﺔ ‪، CPAP ،SIMV‬ﺑﺸﻜﻞ ﻏﻴﺮ ﺟﺮﺍﺣﻲ (ﺑﻮﺍﺳﻄﺔ ﻗﻨﺎﻉ) ﻋﺒﺮ ﺍﻟﻤﺴﺎﻋﺪﺓ‪/‬ﺍﻟﺘﺤﻜﻢ‬

‫‪.‬ﺗﻢﺗﺼﻤﻴﻢ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻠﺮﻋﺎﻳﺔ ﺍﻟﺤﺮﺟﺔ ﻟﻼﺳﺘﺨﺪﺍﻡ ﻓﻲ ﺍﻟﻤﺴﺘﺸﻔﻴﺎﺕ ﻭﺍﻟﻤﺮﺍﻓﻖ ﻣﻦ ﻧﻮﻉ ﺍﻟﻤﺴﺘﺸﻔﻴﺎﺕ‬
‫‪.‬ﻭﻳﻤﻜﻦﺍﺳﺘﺨﺪﺍﻣﻪ ﺃﺛﻨﺎء ﺍﻟﻨﻘﻞ ﺩﺍﺧﻞ ﺍﻟﻤﺴﺘﺸﻔﻰ ﺑﺸﺮﻁ ﺗﻮﻓﻴﺮ ﺍﻟﻄﺎﻗﺔ ﺍﻟﻜﻬﺮﺑﺎﺉﻴﺔ‬

‫ﻣﻮﺍﻧﻊ‪1.7‬‬

‫ﻣﻊﺧﻄﺮ ﺍﻻﻧﻔﺠﺎﺭ‪ .‬ﻻ‬

‫ﺑﻴﺉﺔﺍﻟﺘﺼﻮﻳﺮ ﺑﺎﻟﺮﻧﻴﻦ ﺍﻟﻤﻐﻨﺎﻃﻴﺴﻲ‪ .‬ﻻ ﺗﺴﺘﺨﺪﻡ‬

‫‪.‬ﻳﻤﻜﻦﺃﻥ ﻳﺆﺩﻱ‬

‫ﻳﺠﺐﺃﻥ ﺗﻜﻮﻥ ﻣﺘﺼﻼ ﻓﻘﻂ ﺏ‬

‫ﺇﻣﺪﺍﺩﺍﺕﺍﻟﺘﻴﺎﺭ ﺍﻟﻜﻬﺮﺑﺎﺉﻲ ﻣﻊ ﺍﻷﺭﺽ ﺍﻟﻮﺍﻗﻴﺔ‪ .‬ﻳﺠﺐ ﺍﺳﺘﺨﺪﺍﻡ ﺳﻠﻚ "ﻣﻦ ﻓﺉﺔ ﺍﻟﻤﺴﺘﺸﻔﻰ" ﻭﺗﻮﺻﻴﻠﻪ ﺑﺠﻬﺎﺯ‬

‫‪.‬ﺃﻭﺟﻤﻴﻊ ﺍﻟﺘﺤﺬﻳﺮﺍﺕ ﺍﻟﺒﻴﺉﻴﺔ‬

‫ﺍﻻﺧﺘﺼﺎﺭﺍﺕ ﻭﺍﻟﺘﻌﺎﺭﻳﻒ‪1.8‬‬

‫)ﺱ(‬ ‫ﻳﻌﻨﻲﺗﻌﻴﻴﻦ ﺍﻟﻘﻴﻤﺔ‬

‫)ﻡ(‬ ‫ﻳﻌﻨﻲﺍﻟﻘﻴﻤﺔ ﺍﻟﻤﻘﺎﺳﺔ‬

‫ﺿﻐﻂﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء ﺍﻹﻳﺠﺎﺑﻲ ﺍﻟﻤﺴﺘﻤﺮ‬ ‫ﺟﻬﺎﺯﺿﻐﻂ ﺍﻟﻤﺠﺮﻯ ﺍﻟﻬﻮﺍﺉﻲ ﺍﻹﻳﺠﺎﺑﻲ ﺍﻟﻤﺴﺘﻤﺮ‬ ‫)‪(S‬‬

‫‪F‬‬ ‫)‪ (S‬ﻣﻌﺪﻝﺍﻟﺘﻨﻔﺲ (ﺍﻟﺘﺮﺩﺩ) ﺑﺎﻟﻨﺒﻀﺔ ﻓﻲ ﺍﻟﺪﻗﻴﻘﺔ‪ ،‬ﺃﻱ ﺃﻭﻗﺎﺕ ﺍﻟﺘﻬﻮﻳﺔ ﻓﻲ ﺍﻟﺪﻗﻴﻘﺔ‬

‫ﺳﺒﻮﻧﺖ‪F‬‬ ‫)‪ (M‬ﺗﺮﺩﺩﺍﻟﺘﻨﻔﺲ ﺍﻟﺘﻠﻘﺎﺉﻲ ﻟﻠﻤﺮﻳﺾ‬

‫ﺍﻟﻤﺠﻤﻮﻉ‪F‬‬ ‫ﻭﻣﻌﺪﻝ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺘﻠﻘﺎﺉﻲ ‪ f‬ﺇﺟﻤﺎﻟﻲﻣﻌﺪﻝ ﺍﻟﺘﻨﻔﺲ‪ ،‬ﺃﻱ ﻣﺠﻤﻮﻉ ﻣﻌﺪﻝ ﺍﻟﺘﻨﻔﺲ‬

‫ﺳﺒﻮﻧﺖ(ﻡ)‪F‬‬

‫ﻳﺎ‪2‬‬ ‫ﺍﻟﺘﺮﻛﻴﺰ‪O‬ﻣﻠﻬﻤﺔ‪2‬‬ ‫)‪(S & M‬‬

‫‪1-8‬‬
 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﺃﻱ‬ ‫)‪ (M‬ﻧﺴﺒﺔﺍﻹﻟﻬﺎﻡ ﺇﻟﻰ ﺍﻟﺰﻓﻴﺮ‬

‫ﺇﻡﻓﻲ‬ ‫)‪ (M‬ﺣﺠﻢﺩﻗﻴﻘﺔ ﺍﻟﺰﻓﻴﺮ‬

‫ﺇﻡﻓﻲﺳﺒﻮﻧﺖ‬ ‫)‪ (M‬ﺣﺠﻢﺍﻟﺪﻗﺎﺉﻖ ﺍﻟﺘﻲ ﻳﺘﻢ ﺍﻟﺘﻨﻔﺲ ﺑﻬﺎﺗﻠﻘﺎﺉﻴًﺎ‬

‫ﺇﻡﻓﻲﺗﺴﺮﻳﺐ‬ ‫)‪ (M‬ﺣﺠﻢﺩﻗﻴﻘﺔ ﺍﻟﺘﺴﺮﺏ‬

‫ﻛﻒ‬ ‫)‪ (M‬ﺿﻐﻂﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء ﻟﻠﻤﺮﻳﺾ‬

‫ﺯﻗﺰﻗﺔ‬ ‫)‪ (S & M‬ﺿﻐﻂﺍﻟﺰﻓﻴﺮ ﺍﻟﻨﻬﺎﺉﻲ ﺍﻹﻳﺠﺎﺑﻲ‪ ،‬ﻭﺍﻟﺬﻱ ﻳﻤﻜﻦ ﺃﻥ ﻳﺤﺴﻦ ﺃﻛﺴﺠﺔ ﺍﻟﻤﺮﻳﺾ‬

‫ﺑﻴﺒﻲ‬ ‫)‪ (M‬ﺍﻟﻀﻐﻂﺍﻹﻳﺠﺎﺑﻲ ﺍﻟﺪﺍﺧﻠﻲ ﻟﻠﺰﻓﻴﺮ‬

‫ﺹﻣﻔﺘﺶ‬
‫(‪ PCV )S‬ﻣﺴﺘﻮﻯﺍﻟﻀﻐﻂ ﺍﻟﻌﻠﻮﻱ ﻓﻲ ﻭﺿﻊ‬

‫ﺹﻳﻘﺼﺪ‬ ‫ﻳﻌﻨﻲﺿﻐﻂ ﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء‪ .‬ﻳﺘﻢ ﺗﺤﺪﻳﺚ ﻫﺬﻩ ﺍﻟﻘﻴﻤﺔ ﻓﻲ ﻧﻬﺎﻳﺔ ﺍﻟﺪﻭﺭﺓ ﺍﻟﺘﻨﻔﺴﻴﺔ ﺍﻷﺧﻴﺮﺓ‪ ،‬ﻭﺑﺎﻟﺘﺎﻟﻲ ﻓﻬﻲﻣﺘﻮﺳﻂ‬

‫)‪ (M‬ﻣﺴﺘﻤﺮ‬

‫ﺹﻗﻤﺔ‬ ‫)‪ (M‬ﻗﻴﻤﺔﺫﺭﻭﺓ ﺿﻐﻂ ﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء ﺧﻼﻝ ﺩﻭﺭﺓ ﺗﻬﻮﻳﺔ ﻭﺍﺣﺪﺓ‬

‫ﺹﺑﻼﺕ‬ ‫)‪ (M‬ﺿﻐﻂﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء ﺍﻟﻨﻬﺎﺉﻲ‬

‫ﺹﺩﻗﻴﻘﺔ‬ ‫)‪ (M‬ﺍﻟﺤﺪﺍﻷﺩﻧﻰ ﻟﻀﻐﻂ ﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء‬

‫‪sens‬ﺹ‬ ‫)‪ (S‬ﺣﺴﺎﺳﻴﺔﺍﻟﻀﻐﻂ‬

‫ﺹﻣﻠﺤﻖ‬ ‫)‪ (S‬ﺩﻋﻢﺍﻟﻀﻐﻂ‬

‫ﺹﻋﺎﻟﻲ‬ ‫‪)APRV )S‬ﻭ ‪ BIVENT‬ﻣﺴﺘﻮﻯﺍﻟﻀﻐﻂ ﺍﻟﻌﻠﻮﻱ ﻓﻲ‬

‫ﺹﻗﻠﻴﻞ‬ ‫‪)APRV )S‬ﻭ ‪ BIVENT‬ﺍﻧﺨﻔﺎﺽﻣﺴﺘﻮﻯ ﺍﻟﻀﻐﻂ ﻓﻲ‬

‫‪imax‬ﺕ‬ ‫)‪ (S‬ﺍﻟﺤﺪﺍﻷﻗﺼﻰ ﻟﻮﻗﺖ ﺍﻟﺸﻬﻴﻖ‬

‫ﺕ ﻣﻔﺘﺶ‬ ‫)‪ (S‬ﻭﻗﺖﺍﻟﺸﻬﻴﻖ‬

‫ﺕﻳﻮﻗﻒ‬ ‫)‪ (S‬ﺯﻣﻦﺗﻮﻗﻒ ﺍﻟﺸﻬﻴﻖ‪ ،‬ﻟﺰﻳﺎﺩﺓ ﺯﻣﻦ ﺍﻟﺸﻬﻴﻖ ﻟﺘﺤﺴﻴﻦ ﺃﻛﺴﺠﺔ ﺍﻟﻤﺮﻳﺾ‬

‫)‪ (S‬ﺍﻟﺰﻧﺎﺩﺣﺴﺐ ﻣﻌﺪﻝ ﺍﻟﺘﺪﻓﻖ‬

‫ﺍﻟﺨﺎﻣﺲﺕ‬ ‫)‪ (S‬ﺣﺠﻢﺍﻟﻤﺪ ﻭﺍﻟﺠﺰﺭ ﻟﻠﺘﻬﻮﻳﺔ ﺍﻟﻤﻴﻜﺎﻧﻴﻜﻴﺔ‬

‫‪te‬ﺍﻟﺨﺎﻣﺲ‬ ‫)‪ (M‬ﺣﺠﻢﺍﻟﻤﺪ ﺍﻟﺰﻓﻴﺮﻱ‬

‫‪ti‬ﺍﻟﺨﺎﻣﺲ‬ ‫)‪ (M‬ﺣﺠﻢﺍﻟﻤﺪ ﻭﺍﻟﺠﺰﺭ ﺍﻟﺸﻬﻴﻖ‬

‫‪sens‬ﻩ‬ ‫)‪ (S‬ﺣﺴﺎﺳﻴﺔﺍﻟﺰﻓﻴﺮ‬

‫‪1-9‬‬
 ‫ﺍﺗﻜﻮ‪2‬‬ ‫ﺷﺮﻛﺔﻧﻬﺎﻳﺔ ﺍﻟﺰﻓﻴﺮ‪2‬ﺍﻟﺘﺮﻛﻴﺰ (ﻡ)‬

‫ﻭﻭﺏ‬ ‫ﻋﻤﻞﺍﻟﺘﻨﻔﺲ (ﻡ)‬

‫ﺕﺝ‬ ‫ﺛﺎﺑﺖﺍﻟﻮﻗﺖ (ﻡ)‬

‫‪٪‬ﺗﺴﺮﻳﺐ‬ ‫ﻧﺴﺒﺔﺍﻟﺘﺴﺮﺏ (ﻡ)‬

‫ﻛﺪﻳﻦ‬ ‫ﺍﻻﻣﺘﺜﺎﻝﺍﻟﺪﻳﻨﺎﻣﻴﻜﻲ (ﻡ)‬

‫ﻛﺴﺘﺎﺗﻴﻚ‬ ‫ﺍﻻﻣﺘﺜﺎﻝﺍﻟﺜﺎﺑﺖ (ﻡ)‬

‫ﺭﻳﻨﺴﺐ‬ ‫ﺍﻟﻤﻘﺎﻭﻣﺔﺍﻟﻤﻠﻬﻤﺔ (ﻡ)‬

‫ﺭﻳﻜﺲ‬ ‫ﻣﻘﺎﻭﻣﺔﺍﻟﺰﻓﻴﺮ (ﻡ)‬

‫ﺍﻟﻤﺮﻥ‬ ‫ﺍﻟﻤﻘﺎﻭﻣﺔﺍﻟﻤﺮﻧﺔ (ﻡ)‬

‫‪IP21‬‬ ‫ﻣﺴﺘﻮﻯﺣﻤﺎﻳﺔ ﺍﻟﺠﺴﻴﻤﺎﺕ ﺍﻟﺼﻠﺒﺔ ‪2‬؛ ﻣﺴﺘﻮﻯ ﺣﻤﺎﻳﺔ ﺩﺧﻮﻝ ﺍﻟﺴﺎﺉﻞ ‪1‬‬

‫ﺍﻟﻮﻇﺎﺉﻒ ﺍﻟﻤﺴﺘﺨﺪﻣﺔ ﺑﺸﻜﻞ ﻣﺘﻜﺮﺭ‪1.9‬‬

‫ﻣﻔﺘﺎﺡ ﺗﺸﻐﻴﻞ‪/‬ﺇﻳﻘﺎﻑ ﺍﻟﺘﺸﻐﻴﻞ )‪(1‬‬

‫ﻗﻢ ﺑﺘﻮﺻﻴﻞ ﺧﺮﺍﻃﻴﻢ ﺍﻟﻤﺮﻳﺾ ﻭﺇﻣﺪﺍﺩﺍﺕ ﺍﻟﻐﺎﺯ )‪(2‬‬
‫ﺍﺧﺘﺒﺎﺭ ﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ )‪(3‬‬

‫ﺍﻹﻋﺪﺍﺩﺍﺕ )‪(4‬‬
‫ﺑﺪء ﺍﻟﺘﻬﻮﻳﺔ‪/‬ﺍﻻﺳﺘﻌﺪﺍﺩ )‪(5‬‬
‫ﺑﻴﺎﻧﺎﺕ ﺍﻟﺮﺻﺪ )‪(6‬‬
‫ﺇﻧﺬﺍﺭ‪ ،‬ﺳﺠﻞ ﺍﻷﺣﺪﺍﺙ‪/‬ﺍﻹﻧﺬﺍﺭ )‪(7‬‬
‫ﺍﻟﻤﻌﺎﻳﺮﺓ )‪(8‬‬
‫ﺍﻟﺘﻨﻈﻴﻒ ﻭﺍﻟﺘﻄﻬﻴﺮ )‪(9‬‬
‫ﻣﻜﻮﻧﺎﺕ ﺩﺍﺉﺮﺓ ﺍﻟﺘﻨﻔﺲ )‪(10‬‬
‫ﻧﻈﺎﻡ ﺍﻟﺘﻮﺻﻴﻼﺕ ﺍﻟﺒﻴﻨﻴﺔ ﻹﻣﺪﺍﺩﺍﺕ ﺍﻟﻐﺎﺯ )‪(11‬‬
‫ﺗﻮﺻﻴﻼﺕ ﺍﻟﻤﺮﻃﺐ ﻭﺍﻟﻨﻈﺎﻡ )‪(12‬‬
‫ﺍﻟﺒﺨﺎﺧﺎﺕ ﻭﺍﻟﻮﺻﻼﺕ ﺍﻟﺒﻴﻨﻴﺔ ﻟﻠﻨﻈﺎﻡ )‪(13‬‬

‫ﺍﻟﺮﻣﻮﺯ‪1.10‬‬

‫ﺑﺪﻻﻣﻦ ﺍﻟﺮﺳﻮﻡ ﺍﻟﺘﻮﺿﻴﺤﻴﺔ‪ ،‬ﻳﻤﻜﻦ ﺍﺳﺘﺨﺪﺍﻡ ﺍﻟﺮﻣﻮﺯ‪ .‬ﻗﺪ ﻻ ﺗﻈﻬﺮ ﺟﻤﻴﻊ ﻫﺬﻩ ﺍﻟﺮﻣﻮﺯ ﺑﺎﻟﻀﺮﻭﺭﺓ ﻋﻠﻰ ﺍﻟﺠﻬﺎﺯ ﺃﻭ ﻓﻲ ﺩﻟﻴﻞ ﺍﻟﻤﺴﺘﺨﺪﻡﻫﺬﺍ‪.‬‬

‫‪:‬ﺍﻟﺮﻣﻮﺯ ﺗﺸﻤﻞ‬

‫‪1-10‬‬
 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﺗﺸﻐﻴﻞ(ﺍﻟﻄﺎﻗﺔ)‬ ‫ﻓﺉﺔﺍﻟﺤﻤﺎﻳﺔ ﺍﻟﻨﻮﻉ ﺏ‬

‫ﺇﻳﻘﺎﻑ(ﺍﻟﻄﺎﻗﺔ)‬ ‫‪ BF‬ﻧﻮﻉﻓﺉﺔ ﺍﻟﺤﻤﺎﻳﺔ‬

‫ﺍﺗﺒﻊﺗﻌﻠﻴﻤﺎﺕ ﺍﻟﺘﺸﻐﻴﻞ‬

‫ﺍﻷﺭﺽﺍﻟﻮﺍﻗﻴﺔ‬ ‫ﺍﻟﺠﻬﺪﺍﻟﺨﻄﻴﺮ‬

‫ﺍﺗﺼﺎﻝﻣﺘﺴﺎﻭﻱ ﺍﻟﺠﻬﺪ‬ ‫ﻣﻜﺒﺮﺍﻟﺼﻮﺕ‬

‫ﻗﻔﻞ‬ ‫ﺍﻟﺼﺎﻧﻊ‬

‫ﺍﻟﻐﺎءﺍﻟﻘﻔﻞ‬ ‫ﺗﺎﺭﻳﺦﺍﻻﻧﺘﺎﺝ‬

‫ﻋﻘﺪﻣﻠﻬﻢ‬ ‫ﺭﻗﻢﺳﺮﻱ‬

‫ﺍﻹﺭﺫﺍﺫ‬ ‫ﻋﻘﺪﺍﻟﺰﻓﻴﺮ‬

‫ﺯﻳﺎﺩﺓﺫﻛﻴﺔ ﻟﻸﻛﺴﺠﻴﻦ‬ ‫ﺍﻹﻟﻬﺎﻡﺍﻟﻴﺪﻭﻱ‬

‫ﺗﻌﻠﻴﻖ‬ ‫ﺗﺠﻤﻴﺪﺍﻟﻤﻮﺟﻲ‬

‫ﺗﻴﺎﺭﻣﺴﺘﻤﺮ‬ ‫‪.‬ﻛﺜﺎﻓﺔﺍﻟﻌﻤﻠﻴﺎﺕ‬ ‫ﺑﻄﺎﺭﻳﺔﺩﺍﺧﻠﻴﺔ‬

‫ﺟﻬﺎﺯﻳﻮ ﺍﺱ ﺑﻲ‬ ‫ﺍﻟﺮﺟﻮﻉﺇﻟﻰ ﺍﻟﻮﺛﺎﺉﻖ‬

‫ﺭﺳﺎﻟﺔﺳﺮﻳﻌﺔ‬ ‫ﺑﺎﻟﻔﻌﻞﻋﻠﻰ ﺍﻻﻧﺘﺮﻧﺖ‬

‫ﻣﺸﻐﻞﺍﻟﺘﺪﻓﻖ‬ ‫ﻣﺸﻐﻞﺍﻟﻀﻐﻂ‬

‫‪1-11‬‬
 ‫ﺍﻟﻜﺒﺎﺭ‬ ‫ﺍﻟﺰﻧﺎﺩﺍﻟﻴﺪﻭﻱ‬

‫‪NIV‬ﺃﻭﺿﺎﻉ‬ ‫ﻃﻔﻞ‬

‫ﺍﻟﻘﺎﺉﻤﺔﺍﻟﺮﺉﻴﺴﻴﺔ‬ ‫ﻭﺳﺎﺉﻂﺍﻟﻐﺎﺯﻳﺔ‬

‫ﺣﺪﻳﺜﻲﺍﻟﻮﻻﺩﺓ‬ ‫ﻣﻔﺘﺎﺡﺻﻤﺖ ﺍﻟﺘﻨﺒﻴﻪ‬

‫ﻻﺗﻌﺪ ﺍﻻﺳﺘﺨﺪﺍﻡ‬ ‫ﺍﻟﺘﺨﻠﺺﻣﻦ ﺍﻟﻨﻔﺎﻳﺎﺕ‬

‫‪ IP21‬ﺣﻤﺎﻳﺔﺍﻟﺪﺧﻮﻝ‬

‫‪ VG70‬ﺩﻟﻴﻞ ﺍﻟﺒﺪء ﺍﻟﺴﺮﻳﻊ ﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪1.11‬‬

‫‪.‬ﻗﻢﺑﻤﺮﺍﺟﻌﺔ ﻛﺎﻓﺔ ﺍﻟﻤﻌﻠﻮﻣﺎﺕ ﺍﻟﻮﺍﺭﺩﺓ ﻓﻲ ﺩﻟﻴﻞ ﺍﻟﺘﺸﻐﻴﻞ ﻗﺒﻞ ﻣﺤﺎﻭﻟﺔ ﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﺍ ﺍﻟﺠﻬﺎﺯ‬

‫ﻗﻢ ﺑﺘﻮﺻﻴﻞ ﻣﺼﺪﺭ ﺍﻟﻄﺎﻗﺔ‪.1‬‬

‫ﻗﻢﺑﺘﻮﺻﻴﻠﻪ ﺑﻤﺼﺪﺭ ﻃﺎﻗﺔ ﺍﻟﺘﻴﺎﺭ ﺍﻟﻤﺘﺮﺩﺩ ﺃﻭ ﻣﺼﺪﺭ ﻃﺎﻗﺔ ﺍﻟﺘﻴﺎﺭ ﺍﻟﻤﺴﺘﻤﺮ ﺃﻭ ﺍﺳﺘﺨﺪﻡ ﺍﻟﺒﻄﺎﺭﻳﺔ‬

‫ﻗﻢ ﺑﺘﻮﺻﻴﻞ ﻣﺼﺪﺭ ﺍﻟﻐﺎﺯ‪.2‬‬

‫ﻗﻢ ﺑﺘﺸﻐﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪.3‬‬

‫‪:‬ﻗﻢﺑﺘﺸﻐﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻣﻦ ﺧﻼﻝ ﺍﻟﺘﺤﻮﻝ ﺇﻟﻰ‬

‫‪1-12‬‬
 ‫ﺍﻟﻤﻘﺪﻣﺔ‪1‬‬

‫ﺍﻻﺧﺘﺒﺎﺭ ﺍﻟﻔﻨﻲ‪.4‬‬

‫ﺍﺧﺘﺒﺎﺭ ﻣﺎ ﻗﺒﻞ ﺍﻻﺳﺘﺨﺪﺍﻡ‪.5‬‬

‫ﺣﺪﺩﻣﺮﻳﻀًﺎﺟﺪﻳﺪًﺍ‪.6‬‬

‫‪1-13‬‬
 ‫ﺗﺤﻀﻴﺮ ﺩﺍﺉﺮﺓ ﺍﻟﻤﺮﻳﺾ‪.7‬‬

‫ﺷﺮﻛﺔ ﺍﻻﺗﺼﺎﻝ‪2‬ﺍﻟﻮﺣﺪﺓ (ﺍﺧﺘﻴﺎﺭﻱ)‪.8‬‬

‫)ﺍﺧﺘﻴﺎﺭﻱ( ‪ IRMA‬ﻗﻢ ﺑﺘﻮﺻﻴﻞ ﻣﺤﻮﻝ ﻣﺠﺮﻯ ﺍﻟﻬﻮﺍء‪.9‬‬

‫ﻗﻢ ﺑﻀﺒﻂ ﺇﻋﺪﺍﺩﺍﺕ ﺍﻟﺘﻬﻮﻳﺔ ﺍﻟﻤﻨﺎﺳﺒﺔ‪.10‬‬

‫‪1-14‬‬
 ‫ﻧﻈﺮﺓ ﻋﺎﻣﺔ ﻋﻠﻰ ﺍﻟﻨﻈﺎﻡ‪2‬‬

‫ﻧﻈﺮﺓ ﻋﺎﻣﺔ ﻋﻠﻰ ﺍﻟﻨﻈﺎﻡ‪2‬‬

‫ﻣﻜﻮﻧﺎﺕ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪2.1‬‬

‫)‪ .(GUI‬ﻳﺘﻜﻮﻥﻧﻈﺎﻡ ﺗﻬﻮﻳﺔ ﺍﻟﻌﻨﺎﻳﺔ ﺍﻟﻤﺮﻛﺰﺓ ﻣﻦ ﻣﻜﻮﻧﻴﻦ ﻣﻄﻠﻮﺑﻴﻦ‪ :‬ﻭﺣﺪﺓ ﺍﻟﺘﺤﻜﻢ ﺍﻟﺮﺉﻴﺴﻴﺔ ﻭﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‬

‫ﺍﻟﻤﻜﻮﻧﺎﺕﺍﻻﺧﺘﻴﺎﺭﻳﺔ ﺍﻟﻤﺘﻮﻓﺮﺓ ﻟﻨﻈﺎﻡ ﺗﻬﻮﻳﺔ ﺍﻟﻌﻨﺎﻳﺔ ﺍﻟﻤﺮﻛﺰﺓ ﻫﻲ‪ :‬ﺍﻟﻌﺮﺑﺔ‪،‬ﺗﺠﻤﻴﻊ ﺍﻟﺒﻄﺎﺭﻳﺔ ﺍﻻﺣﺘﻴﺎﻃﻴﺔ‪,‬ﺫﺭﺍﻉ ﺗﺤﺪﻳﺪ ﻣﻮﺿﻊ ﺩﺍﺉﺮﺓﺍﻟﻤﺮﻳﺾ‪،‬‬

‫ﻭ‪2‬‬ ‫‪.‬ﻭﺣﺪﺓ‪ ،‬ﺍﻟﺦ‪CO‬ﻭﺗﺠﻤﻴﻌﺎﺕ ﺩﺍﺉﺮﺓ ﺍﻟﻤﺮﻳﺾ‪،‬‬

‫‪ VG70‬ﺍﻟﺸﻜﻞ‪ 2-1‬ﻣﻠﻒ ﺗﻌﺮﻳﻒ‬

‫‪1‬‬ ‫ﻭﺣﺪﺓﺍﻟﺘﺤﻜﻢ ﺍﻟﺮﺉﻴﺴﻴﺔ‬ ‫‪2‬‬ ‫‪ 3‬ﺍﻟﻤﺮﻃﺐ‬ ‫ﺩﺍﺉﺮﺓﺍﻟﻤﺮﻳﺾ‬

‫‪4‬‬ ‫ﻣﺼﻴﺪﺓﺍﻟﻤﻴﺎﻩ‬ ‫‪5‬‬ ‫‪ 6‬ﺃﻧﺒﻮﺏﺍﻟﺒﺨﺎﺧﺎﺕ‬ ‫‪ Y‬ﻗﻄﻌﺔﻋﻠﻰ ﺷﻜﻞ ﺣﺮﻑ‬

‫‪7‬‬ ‫ﺍﺧﺘﺒﺎﺭﺍﻟﺮﺉﺔ‬ ‫‪8‬‬ ‫‪ 9‬ﻗﻨﺎﻉ‬ ‫ﻣﻮﺻﻞ‬

‫‪10‬‬ ‫ﻣﻮﺻﻞﺍﻟﺒﺨﺎﺧﺎﺕ‬ ‫‪11‬‬ ‫ﺩﺍﺉﺮﺓﺍﻟﻤﺮﻳﺾ‬

‫ﺗﺤﺪﻳﺪﺍﻟﻤﻮﺍﻗﻊ ﺍﻟﺬﺭﺍﻉ‬

‫ﺗﺘﺤﻜﻢﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ ﻓﻲ ﺇﻋﺪﺍﺩﺍﺕ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ :‬ﻳﻤﻜﻦ ﺗﺤﺪﻳﺪ ﺍﻹﻋﺪﺍﺩﺍﺕ ﻭﺿﺒﻄﻬﺎ ﺑﺎﺳﺘﺨﺪﺍﻡ ﺇﺻﺒﻊ ﻋﻠﻰﺍﻟﺸﺎﺷﺔ ﻭ‪/‬ﺃﻭ‬

‫ﻣﻘﺒﺾ ﺟﻬﺎﺯ ﺍﻟﺘﺸﻔﻴﺮ‪ .‬ﺗﺘﺤﻘﻖ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ ﻣﻦ ﺇﻣﻜﺎﻧﻴﺔ ﺍﻟﺤﺼﻮﻝ ﻋﻠﻰ ﺟﻤﻴﻊ ﻣﺠﻤﻮﻋﺎﺕ ﺍﻹﻋﺪﺍﺩﺍﺕﻭﺳﺘﻘﻮﻡ ﺑﺈﻋﻼﻡ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺑﺄﻱ‬

‫‪.‬ﻗﻴﻮﺩ ﻋﻠﻰ ﺍﻹﻋﺪﺍﺩﺍﺕ‬

‫‪2-1‬‬
 ‫ﻳﺘﻢﻗﻴﺎﺱ ﻣﻌﻠﻤﺎﺕ ﺍﻟﺘﻨﻔﺲ ﺑﺸﻜﻞ ﻣﺴﺘﻤﺮ ﺑﻮﺍﺳﻄﺔ ﻣﺤﻮﻻﺕ ﺍﻟﻄﺎﻗﺔ ﻭﻳﺘﻢ ﺍﻟﺘﺤﻜﻢ ﻓﻴﻬﺎ ﺑﻮﺍﺳﻄﺔ ﻧﻈﺎﻡ ﺍﻟﺘﻐﺬﻳﺔ ﺍﻟﻤﺮﺗﺪﺓ ﻓﻲﻭﺣﺪﺓ ﺗﻮﺻﻴﻞ ﺍﻟﺘﻨﻔﺲ‪.‬‬

‫ﻳﺴﺘﺠﻴﺐ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻼﺧﺘﻼﻑ ﺑﻴﻦ ﺍﻟﻘﻴﻤﺔ ﺍﻟﻤﻘﺎﺳﺔ ﺍﻟﻔﻌﻠﻴﺔ ﻟﻠﻤﻌﻠﻤﺔ ﻭﺍﻟﻘﻴﻤﺔ ﺍﻟﻤﺤﺪﺩﺓﻣﺴﺒﻘًﺎ ﺃﻭ ﺍﻟﻤﺤﺴﻮﺑﺔ ﻋﻦ ﻃﺮﻳﻖ ﺿﺒﻂ‬

‫‪.‬ﺗﻮﺻﻴﻞ ﺍﻟﻐﺎﺯ ﻟﺘﺤﻘﻴﻖ ﺍﻟﻘﻴﻤﺔ ﺍﻟﻤﺴﺘﻬﺪﻓﺔ‬

‫ﻣﻜﻮﻧﺎﺕ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ‪2.2‬‬

‫ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‪2.2.1‬‬

‫ﺍﻟﺸﻜﻞ‪ 2-2‬ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‬

‫ﻣﺼﺒﺎﺡ ﺍﻟﺘﻨﺒﻴﻪ‪.1‬‬

‫ﺷﺎﺷﺔ ﺍﻟﻠﻤﺲ‪.2‬‬

‫ﻣﻘﺒﺾ ﺍﻟﺘﺸﻔﻴﺮ‪.3‬‬

‫ﻣﻔﺘﺎﺡ ﺍﻟﺼﻤﺖ ﺍﻟﺘﻨﺒﻴﻪ ﺍﻟﺜﺎﺑﺖ‪.4‬‬

‫ﻳﻤﻜّﻦﺍﻟﻤﻔﺘﺎﺡ ﺍﻟﺜﺎﺑﺖ ﻟﻜﺘﻢ ﺻﻮﺕ ﺍﻹﻧﺬﺍﺭ ﺍﻟﻤﺴﺘﺨﺪﻡ ﻣﻦ ﺇﺳﻜﺎﺕ ﺍﻹﻧﺬﺍﺭﺍﺕ ﻟﻤﺪﺓ ﺩﻗﻴﻘﺘﻴﻦ‪ .‬ﺳﻴﺆﺩﻱ ﺍﻟﻀﻐﻂ ﻋﻠﻰ ﻣﻮﻗﻊ ﻣﺎﻋﻠﻰ ﺷﺎﺷﺔ ﻭﺍﺟﻬﺔ‬
‫ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ ﺇﻟﻰ ﻇﻬﻮﺭ ﻗﺎﺉﻤﺔ ﻓﺮﻋﻴﺔ ﺃﻭ ﺗﻤﻴﻴﺰ ﻣﻌﻠﻤﺔ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﺃﻭ ﻣﻔﺘﺎﺡ ﺍﻻﺧﺘﺼﺎﺭ‪.‬ﻳﺆﺩﻱ ﺗﺪﻭﻳﺮ ﻣﻘﺒﺾ ﺍﻟﺘﺸﻔﻴﺮ ﻋﻨﺪ‬
‫‪.‬ﺗﺤﺪﻳﺪ ﻣﻌﻠﻤﺔ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﺇﻟﻰ ﺍﻟﺴﻤﺎﺡ ﻟﻠﻤﺴﺘﺨﺪﻡ ﺑﺎﻟﺘﻤﺮﻳﺮ ﻋﺒﺮ ﺍﻟﻨﻄﺎﻕﺍﻟﻤﺘﺎﺡ‬

‫‪2-2‬‬
 ‫ﻧﻈﺮﺓ ﻋﺎﻣﺔ ﻋﻠﻰ ﺍﻟﻨﻈﺎﻡ‪2‬‬

‫ﺍﻟﻠﻮﺣﺔ ﺍﻟﺠﺎﻧﺒﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‪2.2.2‬‬

‫ﺍﻟﺸﻜﻞ‪ 2-3‬ﺍﻟﻠﻮﺣﺔ ﺍﻟﺠﺎﻧﺒﻴﺔ ﻟﺸﺎﺷﺔ ﻭﺍﺟﻬﺔ ﺍﻟﻤﺴﺘﺨﺪﻡ ﺍﻟﺮﺳﻮﻣﻴﺔ‬

‫‪.‬ﻭﺣﺪﺓﺍﻟﺘﺤﻜﻢ‬

‫‪.‬ﺃﻭﻗﻴﺪ ﺍﻟﺘﺸﻐﻴﻞ‬

‫ﺍﻟﺘﻲ ﺳﺘﻌﺮﺽ ﻧﻔﺲ ﺍﻟﻤﻌﻠﻮﻣﺎﺕ ‪ VGA‬ﻟﺘﻮﺻﻴﻞ ﺷﺎﺷﺔ‪ :VGA‬ﻭﺍﺟﻬﺔ‪.2‬‬

‫‪.‬ﺩ‬

‫‪.‬ﻡﻗﻴﺪ ﺍﻻﺳﺘﺨﺪﺍﻡ ﻋﻠﻰ ﺍﻟﻤﺮﻳﺾ‬

‫ﻳُﺴﻤﺢ‪ :‬ﻓﻘﻂ ﺑﺄﺟﻬﺰﺓ ﺍﻟﺘﺨﺰﻳﻦ ﺍﻟﺨﺎﺭﺟﻴﺔ ﺫﺍﺕ ﺍﺳﺘﻬﻼﻙ ﺍﻟﻄﺎﻗﺔ ﺍﻟﻤﻨﺨﻔﺾ‪ USB‬ﻭﺍﺟﻬﺔ‪.3‬‬

‫‪.‬ﺍﻟﻨﻈﺎﻡﻓﻲ ﺍﻟﺨﺪﻣﺔ‬

‫‪.‬ﻭﺍﺟﻬﺔ ﺍﻟﺸﺒﻜﺔ‪:‬ﻟﻼﺗﺼﺎﻝ ﺑﺎﻟﻤﻌﺪﺍﺕ ﺍﻟﺨﺎﺭﺟﻴﺔ ﻣﺜﻞ ﺍﻟﺴﺠﻞ ﺍﻟﺼﺤﻲ ﺍﻹﻟﻜﺘﺮﻭﻧﻲ‪.4‬‬

‫‪..‬ﺧﻄﺒﺔ‬

‫‪.‬ﻳﻤﻜﻦﻟﻠﻤﻮﻇﻔﻴﻦ ﺍﻟﻤﻌﺘﻤﺪﻳﻦ ﺍﺳﺘﺨﺪﺍﻣﻪ‬

‫‪2-3‬‬
 ‫ﻭﺣﺪﺓ ﺍﻟﺘﺤﻜﻢ ﺍﻟﺮﺉﻴﺴﻴﺔ‪2.3‬‬

‫ﻭﺣﺪﺓﺍﻟﺘﺤﻜﻢ ﺍﻟﺮﺉﻴﺴﻴﺔ ﻫﻲ ﺍﻟﻤﺴﺆﻭﻟﺔ ﻋﻦ ﺍﻟﺘﺤﻜﻢ ﻓﻲ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ .‬ﻟﺪﻳﻬﺎ ﻭﺍﺟﻬﺎﺕ ﻋﻠﻰ ﺍﻷﻟﻮﺍﺡ ﺍﻷﻣﺎﻣﻴﺔ ﻭﺍﻟﺨﻠﻔﻴﺔﺑﻤﺎ ﻓﻲ ﺫﻟﻚ‬

‫‪.‬ﻭﺍﺟﻬﺎﺕ ﻫﻮﺍﺉﻴﺔ ﻭﺇﻟﻜﺘﺮﻭﻧﻴﺔ‬

‫ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ‪2.3.1‬‬

‫ﺍﻟﺸﻜﻞ‪ 2-4‬ﺍﻟﻠﻮﺣﺔ ﺍﻷﻣﺎﻣﻴﺔ‬

‫ﻭﺣﺪﺓ ﺍﻟﺰﻓﻴﺮ‪:‬ﻹﺯﺍﻟﺔ ﻭﺣﺪﺓ ﺍﻟﺰﻓﻴﺮ‪ :‬ﺍﺿﻐﻂ ﻋﻠﻰ ﺍﻟﻤﺰﻻﺝ (‪ )5‬ﺍﻟﻤﻮﺟﻮﺩ ﻋﻠﻰ ﺍﻟﺠﺰء ﺍﻷﻳﻤﻦ ﻣﻦ ﺍﻟﻐﻄﺎء ﺍﻷﻣﺎﻣﻲ (ﺃﻱ ﺍﻓﺘﺤﻪ) ﺛﻢﺃﺧﺮﺝ ﻭﺣﺪﺓ‪.1‬‬

‫ﺍﻟﺰﻓﻴﺮ‪ .‬ﺑﻌﺪ ﺍﻟﺘﻨﻈﻴﻒ ﺃﻭ ﺍﻟﺘﻄﻬﻴﺮ ﻋﺎﻟﻲ ﺍﻟﻤﺴﺘﻮﻯ‪ ،‬ﺃﺩﺧﻞ ﺍﻟﻮﺣﺪﺓ ﻓﻲ ﺍﻟﻤﻮﺿﻊ ﺍﻟﻤﻨﺎﺳﺐ ﺣﺘﻰ ﻳﻌﻮﺩ ﻣﺰﻻﺝ ﺍﻟﻘﻔﻞﺇﻟﻰ ﻣﻜﺎﻧﻪ‬

‫ﻟﺘﺠﻨﺐﺍﻟﺘﺴﺮﺏ‪ .‬ﻧﻈﺎﻡ‬

‫ﺹﺍﻟﺘﻜﺜﻴﻒ‪ ،‬ﺗﻮﺧﻲ ﺍﻟﺤﺬﺭ‬

‫‪.‬ﺑﺴﺒﺐﺍﺭﺗﻔﺎﻉ ﺩﺭﺟﺔ ﺍﻟﺤﺮﺍﺭﺓ‬

‫‪.‬ﻣﻨﻔﺬ ﺍﻟﻌﺎﺩﻡ‪:‬ﻳﺘﻢ ﺇﻃﻼﻕ ﻏﺎﺯ ﺍﻟﺰﻓﻴﺮ ﻟﻠﻤﺮﻳﺾ ﻣﻦ ﺧﻼﻝ ﻫﺬﺍ ﺍﻟﻤﻨﻔﺬ ﺇﻟﻰ ﻫﻮﺍء ﺍﻟﻐﺮﻓﺔ‪.2‬‬

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 ‫ﻧﻈﺮﺓ ﻋﺎﻣﺔ ﻋﻠﻰ ﺍﻟﻨﻈﺎﻡ‪2‬‬

‫‪ ruit‬ﺇﻟﻰﻫﺬﺍ ﺍﻟﻤﻨﻔﺬ‪.‬‬

‫‪.‬ﺃﻭﺭﺕ‬

‫‪.‬ﻛﻮﺏ ﻣﺼﻴﺪﺓ ﺍﻟﻤﺎء‪:‬ﺟﻤﻊ ﺍﻟﻤﺎء ﺍﻟﻤﻜﺜﻒ ﻟﻤﻨﻌﻪ ﻣﻦ ﺍﻟﺪﺧﻮﻝ ﺇﻟﻰ ﺻﻤﺎﻡ ﺍﻟﺰﻓﻴﺮ‪.4‬‬

‫‪.‬ﻭﺣﺪﺓﺍﻟﺰﻓﻴﺮ‬

‫ﻭﺣﺪﺓﺍﻟﺰﻓﻴﺮ ﺑﻴﻨﻤﺎ‬
‫‪.‬ﺟﻬﺎﺯﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻗﻴﺪ ﺍﻻﺳﺘﺨﺪﺍﻡ ﻋﻠﻰ ﺍﻟﻤﺮﻳﺾ‬

‫‪.‬ﻣﻨﻔﺬ ﺇﺧﺮﺍﺝ ﺍﻟﺒﺨﺎﺧﺎﺕ‪:‬ﻟﺘﻮﺻﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺒﺨﺎﺧﺎﺕ‪.6‬‬

‫ﻏﻄﺎء ﺣﺴﺎﺱ ﺍﻷﻭﻛﺴﺠﻴﻦ‪.7‬‬

‫‪.‬ﺧﺮﻃﻮﻡﺍﻷﻃﺮﺍﻑ ﺍﻟﻤﻠﻬﻤﺔ‬

‫‪.‬ﺃﻭﺭﺕ‬

‫ﺍﻟﻠﻮﺣﺔ ﺍﻟﺨﻠﻔﻴﺔ‪2.3.2‬‬

‫ﺍﻟﺸﻜﻞ‪ 2-5‬ﺍﻟﻠﻮﺣﺔ ﺍﻟﺨﻠﻔﻴﺔ‬

‫‪2-5‬‬
 ‫‪1‬‬ ‫ﻏﻄﺎءﺍﻟﺒﻄﺎﺭﻳﺔ‬ ‫‪2‬‬ ‫ﺷﺮﻛﺔ‪2‬ﻣﻮﺻﻞ ﺍﻟﻮﺣﺪﺓ‬ ‫‪3‬‬ ‫ﻣﻮﺻﻞﺍﺳﺘﺪﻋﺎء ﺍﻟﻤﻤﺮﺿﺔ‬

‫‪4‬‬ ‫ﻣﺪﺧﻞﺍﻟﻬﻮﺍء‬ ‫‪5‬‬ ‫ﻣﺪﺧﻞﺍﻷﻛﺴﺠﻴﻦ ﻣﻨﺨﻔﺾ ﺍﻟﺘﺪﻓﻖ‬ ‫‪6‬‬ ‫ﻣﺪﺧﻞﺍﻷﻛﺴﺠﻴﻦ ﻋﺎﻟﻲ ﺍﻟﻀﻐﻂ‬

‫‪7‬‬ ‫ﻣﺮﻭﺣﺔﺗﺒﺮﻳﺪ‬ ‫‪8‬‬ ‫ﻓﻴﻮﺯﻃﺎﻗﺔ ﺍﻟﺘﻴﺎﺭ ﺍﻟﻤﺴﺘﻤﺮ‬ ‫‪9‬‬ ‫ﻣﻨﻔﺬﺇﺩﺧﺎﻝ ﺍﻟﻄﺎﻗﺔ ﺑﺎﻟﺘﻴﺎﺭ ﺍﻟﻤﺴﺘﻤﺮ‬

‫‪10‬‬ ‫ﻣﺘﺴﺎﻭﻳﺔﺍﻟﺠﻬﺪﺻﺎﻟﺔ‬ ‫‪11‬‬ ‫ﻣﻘﺒﺲﺇﻣﺪﺍﺩ ﺍﻟﻄﺎﻗﺔ‬ ‫‪12‬‬ ‫ﻣﻔﺘﺎﺡﺇﻣﺪﺍﺩ ﺍﻟﻄﺎﻗﺔ‬

‫ﺭﺑﻂﺃﺟﺰﺍء ﻣﺨﺘﻠﻔﺔ ﻣﻦ‬

‫ﺍﻟﻤﻌﺪﺍﺕﺃﻭ ﻧﻈﺎﻡ ﺍﻟﻤﻌﺪﺍﺕ ﺍﻟﻄﺒﻴﺔ ﻟﻨﻔﺲ ﺍﻹﻣﻜﺎﻧﺎﺕ‪ .‬ﻋﻨﺪ ﺗﻮﺻﻴﻠﻪ‪ ،‬ﻳﺠﺐ‬

‫ﻭﻣﺪﺧﻞﺍﻟﻬﻮﺍء! ﻧﻈﻒ ﺍﻝ‬

‫ﺗﺼﻔﻴﺔﺑﺎﻧﺘﻈﺎﻡ! ﻻ ﻳﻨﺒﻐﻲ ﺗﻐﻄﻴﺔ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﺃﻭ ﻭﺿﻌﻪ ﺑﻄﺮﻳﻘﺔ ﺗﺆﺛﺮﺳﻠﺒﺎً ﻋﻠﻰ ﺗﺸﻐﻴﻞ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲﺃﻭ ﺃﺩﺍﺉﻪ‬
‫(ﻋﻠﻰ ﺳﺒﻴﻞ ﺍﻟﻤﺜﺎﻝ‪ ،‬ﻭﺿﻌﻪ ﺑﺠﻮﺍﺭ‬
‫‪ tilator‬ﻻﺭﺗﻔﺎﻉ ﺩﺭﺟﺔ ﺍﻟﺤﺮﺍﺭﺓ)‪.‬‬

‫‪.‬ﺃﻭﺍﻟﻤﻜﻮﻧﺎﺕ ﺍﻟﻘﺎﺑﻠﺔ ﻟﻠﺘﻠﻒ‬

‫ﺷﺮﻛﺔ‪2‬ﻭﺣﺪﺓ‪ ،‬ﻭﻻ ﻳﻤﻜﻦ ﺃﻥ ﻳﻜﻮﻥ‬

‫‪.‬ﻣﺘﺼﻠﺔﻣﻊ ﺍﻟﻤﻨﺎﻓﺬ ﺍﻟﺘﺴﻠﺴﻠﻴﺔ ﺍﻷﺧﺮﻯ‬

‫ﺍﻟﻌﺮﺑﺔ‪2.4‬‬

‫ﻳﻤﻜﻦﺍﺳﺘﺨﺪﺍﻡ ﻋﺮﺑﺔ ﺍﺧﺘﻴﺎﺭﻳﺔ ﻟﺘﺮﻛﻴﺐ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪ .‬ﻳﻨﻄﺒﻖ ﺫﻟﻚ ﻋﻠﻰ ﻭﺿﻊ ﻭﺗﺤﺮﻳﻚ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪.‬ﺗﺤﺘﻮﻱ‬

‫‪.‬ﺍﻟﻌﺮﺑﺔ ﻋﻠﻰ ﻟﻮﺣﺔ ﺗﻜﻴﻴﻒ ﻣﺴﺎﻋﺪﺓ‬

‫ﺍﻟﻤﺮﻃﺐ‪2.5‬‬

‫ﺃﻭ ﻣﻨﺘﺞ ﻣﺸﺎﺑﻪ‪ ،‬ﻣﻊ ﺟﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ‪.‬ﻗﺪ ﺗﻘﻮﻡ ‪ Fisher & Paykel MR850،‬ﻳﻨﺒﻐﻲﺍﺳﺘﺨﺪﺍﻡ ﺟﻬﺎﺯ ﺗﺮﻃﻴﺐ ﺍﺧﺘﻴﺎﺭﻱ‪ ،‬ﻣﺜﻞ‬

‫‪.‬ﺷﺮﻛﺘﻨﺎ ﺑﺘﻮﺭﻳﺪ ﺃﺟﻬﺰﺓ ﺗﺮﻃﻴﺐ ﺍﻟﻬﻮﺍء ﻓﻲ ﻣﻨﻄﻘﺘﻚ ‪ -‬ﺗﺤﺪﺙ ﻣﻊ ﻣﻨﺪﻭﺏ ﻣﺒﻴﻌﺎﺕ ﺷﺮﻛﺘﻨﺎ ﺇﺫﺍ ﻛﻨﺖ ﺑﺤﺎﺟﺔﺇﻟﻰ ﻣﺰﻳﺪ ﻣﻦ ﺍﻟﻤﻌﻠﻮﻣﺎﺕ‬

‫ﻃﻘﻢﺳﻠﻨﺪﺭ ‪2.6‬‬

‫‪ .(2US E )O‬ﺗﺘﻮﻓﺮﻣﺠﻤﻮﻋﺔ ﺗﺮﻛﻴﺐ ﺃﺳﻄﻮﺍﻧﺔ ﺍﻟﻐﺎﺯ ﺍﻻﺧﺘﻴﺎﺭﻳﺔ ﺍﻟﺘﻲ ﺗﺤﺘﻮﻱ ﻋﻠﻰ ﺃﺳﻄﻮﺍﻧﺘﻴﻦ ﻣﻦ ﻧﻮﻉ‬

‫‪2-6‬‬
 ‫ﻛﻮ‪2‬ﻭﺣﺪﺓ‪3‬‬

‫ﻛﻮ‪2‬ﻭﺣﺪﺓ‪3‬‬

‫ﺛﺎﻧﻲ ﺃﻛﺴﻴﺪ ﺍﻟﻜﺮﺑﻮﻥ‪2‬ﺍﻻﺳﺘﺨﺪﺍﻡ ﺍﻟﻤﻘﺼﻮﺩ ﻟﻠﻮﺣﺪﺓ‪3.1‬‬

‫ﺍﻟﺸﺮﻛﺔﺍﻟﺴﺎﺉﺪﺓ‪ 2‬ﺗﻢ ﺗﺼﻤﻴﻢ ﺍﻟﻮﺣﺪﺓ ﻟﻴﺘﻢ ﺗﻮﺻﻴﻠﻬﺎ ﺑﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺲ ﺍﻟﺼﻨﺎﻋﻲ ﻟﻌﺮﺽ ﺑﻴﺎﻧﺎﺕ ﺍﻟﻤﺮﺍﻗﺒﺔ ﺍﻟﻤﺸﺘﻘﺔ ﻓﻲ ﺍﻟﻮﻗﺖﺍﻟﻔﻌﻠﻲ ﻟﺜﺎﻧﻲ‬

‫ﺍﻟﻜﺮﺑﻮﻥ‪2.‬‬ ‫ﺃﻛﺴﻴﺪ‬

‫ﺍﻟﺸﺮﻛﺔﺍﻟﺴﺎﺉﺪﺓ‪ 2‬ﺗﻢ ﺗﺼﻤﻴﻢ ﺍﻟﻮﺣﺪﺓ ﻟﻴﺘﻢ ﺗﻮﺻﻴﻠﻬﺎ ﺑﺪﺍﺉﺮﺓ ﺗﻨﻔﺲ ﺍﻟﻤﺮﻳﺾ ﻟﻤﺮﺍﻗﺒﺔ ﺍﻟﻐﺎﺯﺍﺕ ﺍﻟﻤﺴﺘﻨﺸﻘﺔ‪/‬ﻣﻨﺘﻬﻴﺔ ﺍﻟﺼﻼﺣﻴﺔﺃﺛﻨﺎء ﺍﻟﺘﻌﺎﻓﻲ‬

‫ﻭﺭﻋﺎﻳﺔ ﺍﻟﺠﻬﺎﺯ ﺍﻟﺘﻨﻔﺴﻲ‪ .‬ﻳﻤﻜﻦ ﺍﺳﺘﺨﺪﺍﻣﻪ ﻓﻲ ﻏﺮﻓﺔ ﺍﻟﻌﻤﻠﻴﺎﺕ ﻭﻭﺣﺪﺓ ﺍﻟﻌﻨﺎﻳﺔ ﺍﻟﻤﺮﻛﺰﺓ ﻭﻏﺮﻓﺔ ﺍﻟﻤﺮﺿﻰﻭﺇﻋﺪﺍﺩﺍﺕ ﻃﺐ ﺍﻟﻄﻮﺍﺭﺉ‬

‫‪.‬ﻟﻠﻤﺮﺿﻰ ﺍﻟﺒﺎﻟﻐﻴﻦ ﻭﺍﻷﻃﻔﺎﻝ‬

‫‪.‬ﺍﻟﺸﺮﻛﺔ‪2‬ﻟﻴﺲ ﺍﻟﻤﻘﺼﻮﺩ ﻣﻦ ﻫﺬﻩ ﺍﻟﻮﺣﺪﺓ ﺃﻥ ﺗﺴﺘﺨﺪﻡ ﻛﻮﺳﻴﻠﺔ ﻭﺣﻴﺪﺓ ﻟﻤﺮﺍﻗﺒﺔ ﺍﻟﻤﺮﻳﺾ‪ .‬ﻭﻳﺠﺐ ﺍﺳﺘﺨﺪﺍﻣﻪﺩﺍﺉﻤًﺎ ﻣﻊ ﺃﻧﻈﻤﺔﺍﻟﻤﺮﺍﻗﺒﺔ ﺍﻟﺒﺪﻳﻠﺔ‬

‫ﺛﺎﻧﻲ ﺃﻛﺴﻴﺪ ﺍﻟﻜﺮﺑﻮﻥ‪2‬ﻣﻮﺍﺻﻔﺎﺕ ﺍﻟﻮﺣﺪﺓ‪3.2‬‬

‫ﻋﺎﻡ‪3.2.1‬‬

‫ﻭﺻﻒ‬ ‫‪2‬‬ ‫‪.‬ﻣﺴﺒﺎﺭ‪CO‬ﻣﻀﻐﻮﻁﻟﻠﻐﺎﻳﺔ ﻳﻨﻔﺎﺭﻳﺪ ﺍﻟﺘﻴﺎﺭ‬

‫ﺍﻷﺑﻌﺎﺩ(ﺍﻟﻌﺮﺽ × ﺍﻟﻌﻤﻖ × ﺍﻻﺭﺗﻔﺎﻉ)‬ ‫)ﻣﻠﻢ ‪ )1.49‬ﺑﻮﺻﺔ ‪ × 1.45‬ﺑﻮﺻﺔ ‪ × 1.34‬ﺑﻮﺻﺔ ‪34 × 37 ×38‬‬

‫ﻃﻮﻝﺍﻟﺴﻠﻚ‬ ‫ﻡ ‪ ± 0.02‬ﻡ‪2.50‬‬

‫ﻭﺯﻥ‬ ‫ﺟﻢ (ﺑﺎﺳﺘﺜﻨﺎء ﺍﻟﻜﺎﺑﻞ) > ‪25‬‬

‫ﺩﺭﺟﺔﺣﺮﺍﺭﺓ ﺍﻟﺘﺸﻐﻴﻞ‬ ‫ﺇﻟﻰ ‪ 40‬ﺩﺭﺟﺔ ﻣﺉﻮﻳﺔ ‪ / 32‬ﺇﻟﻰ ‪ 104‬ﺩﺭﺟﺔ ﻓﻬﺮﻧﻬﺎﻳﺖ ‪0‬‬

‫ﺩﺭﺟﺔﺣﺮﺍﺭﺓ ﺍﻟﺘﺨﺰﻳﻦ ﻭﺍﻟﻨﻘﻞ‬ ‫ﺇﻟﻰ ‪ 75‬ﺩﺭﺟﺔ ﻣﺉﻮﻳﺔ‪ -40 ،‬ﺇﻟﻰ ‪ 167‬ﺩﺭﺟﺔ ﻓﻬﺮﻧﻬﺎﻳﺖ ‪40-‬‬

‫ﺭﻃﻮﺑﺔﺍﻟﻌﻤﻠﻴﺔ‬ ‫ﺇﻟﻰ ‪ 95%‬ﺭﻃﻮﺑﺔ ﻧﺴﺒﻴﺔ‪ ،‬ﻏﻴﺮ ﻣﻜﺜﻔﺔ‪10‬‬

‫ﺭﻃﻮﺑﺔﺍﻟﺘﺨﺰﻳﻦ ﻭﺍﻟﻨﻘﻞ‬ ‫ﻣﻜﺜﻔﺔ( ‪1‬‬ ‫ﺭﻃﻮﺑﺔﻧﺴﺒﻴﺔ ﻣﻦ ‪ 5‬ﺇﻟﻰ ‪،100%‬‬

‫ﺇﻟﻰ ‪ 1200‬ﻫﻜﺘﻮﺑﺎﺳﻜﺎﻝ ‪ )525‬ﻫﻜﺘﻮﺑﺎﺳﻜﺎﻝ ﺍﻟﻤﻮﺍﻓﻖ ﻻﺭﺗﻔﺎﻉ‪525‬‬

‫ﺍﻟﺘﺸﻐﻴﻞﺍﻟﻀﻐﻂ ﺍﻟﺠﻮﻱ‬
‫)ﻡ ‪ / 15000‬ﻗﺪﻡ‪4572‬‬

‫ﺿﻐﻂﺍﻟﺘﺨﺰﻳﻦ ﻭﺍﻟﻨﻘﻞ‬ ‫ﺇﻟﻰ ‪ 1200‬ﻫﺒﺄ‪500‬‬

 ‫‪.‬ﻳﺘﺤﻤﻞﺍﻟﺴﻘﻮﻁ ﺍﻟﻤﺘﻜﺮﺭ ﻟﻤﺴﺎﻓﺔ ‪ 1.8‬ﻣﺘﺮ ﻋﻠﻰ ﺳﻄﺢ ﺻﻠﺐ‬
‫ﺍﻟﻘﻮﺓﺍﻟﻤﻴﻜﺎﻧﻴﻜﻴﺔ‬
‫ﻳﺘﻮﺍﻓﻖﻣﻊ ﻣﺘﻄﻠﺒﺎﺕ ﺳﻴﺎﺭﺍﺕ ﺍﻹﺳﻌﺎﻑ ﻋﻠﻰ ﺍﻟﻄﺮﻕ‬

‫‪3-1‬‬