Aircraft Medical McGRATH MAC EMS Panduan Operator - Halaman 14

Jelajahi secara online atau unduh pdf Panduan Operator untuk Peralatan Medis Aircraft Medical McGRATH MAC EMS. Aircraft Medical McGRATH MAC EMS 19 halaman. Video laryngoscope

Aircraft Medical McGRATH MAC EMS Panduan Operator
3.4 High-Level Disinfection
AUTOMATED CHEMICAL DISINFECTOR
McGRATH® MAC EMS with McGRATH® 3.6V EMS
Battery removed
The McGRATH® MAC EMS is suitable for reprocessing in STERIS® SYSTEM 1E.
Follow STERIS® instructions for processing using SYSTEM 1E.
HIGH-LEVEL DISINFECTANT IMMERSION
McGRATH® MAC EMS with McGRATH® 3.6V EMS
Battery removed
Ensure that the device has been thoroughly cleaned, rinsed and dried prior to disinfection.
Disinfect the device in accordance with the high-level disinfectant manufacturer's instructions
The process below has been approved by Aircraft Medical using ASP Cidex OPA:
Ensure that the disinfectant receptacle is clean and dry. Wearing appropriate personal
protective equipment, fill the receptacle with sufficient prepared disinfectant solution
so as to ensure complete immersion of the device. Carefully immerse the device in the
solution in such a way as to displace any trapped air within the device; it is important to
ensure that the solution reaches all surfaces. Place the lid on the receptacle and leave for
12 minutes.
Remove the device from the solution, drain into receptacle before transferring to clean
rinse receptacle. Rinse thoroughly with sterile water of suitable microbiological quality.
Remove device from rinse solution and drain.
Carefully hand-dry using clean, absorbent, non-shedding cloth.
A Chemical Compatibility List is available which lists other high-level disinfectants that have
been approved by Aircraft Medical as compatible and will cause no physical degradation to
the McGRATH® MAC EMS. Aircraft Medical make no claims regarding the efficacy of the other
disinfectants listed. Please consult the disinfectant manufacturer's instructions and guidelines.
Ensure that the chemicals are not harmful to the patient or user and that they have been
approved by the relevant decontamination authority.
13