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Cleaning, Disinfection and Sterilization
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 7.2  Disinfection and Sterilization Procedure for Lip Clip,   Operation  Operating mode  Warning
 Connection Hook and Fork
                               •  Inspect devices and   •  Dirty instruments must be
 Foreword                        sort out those with    cleaned and disinfected
                                 defects.               again.
 For hygiene and sanitary safety purposes, the lip clip, the connection   •  Assemble the devices   •  Discard instruments which
 hook and the fork must be cleaned, disinfected and sterilized before   (stops).  show any deformations
 each usage to prevent any cross-contamination between patients. This   (bent, twisted), damages
 concerns the first use as well as the subsequent uses.  (broken, corroded) or defects
           7   Inspection
 General recommendations                                (loss of colour coding or
 •  Use only a disinfecting solution which is approved for its efficacy   marking) affecting the
 (VAH/DGHM-listing, CE marking, FDA approval) and in accordance   resistance, the safety or the
                                                        performance of the
 with the DFU of the disinfecting solution manufacturer. For all metal   instrument.
 instruments, it is recommended to use anticorrosion disinfecting   •  Do not use instrument
 and cleaning agents;                                   lubricants.
 •  For your own safety, please wear personal protective equipment   •  Place the devices in a   •  Avoid any contact between
 (gloves, glasses, mask).        support or container   instruments during
 •  The user is responsible for the sterility of the product for the first   to avoid any contact   sterilization. Use supports or
 cycle and each further usage as well as for the usage of damaged   between instruments   containers.
 or dirty instruments where applicable after sterility.  or posts and pack the   •  Check the validity period of
 •  Limitations and restrictions on reprocessing:   devices in   the pouch given by the
 the appearance of defects such as cracks, deformations (bent,   8  Packaging  “Sterilization   manufacturer to determine
 twisted), corrosion, loss of colour coding or marking, are indications   pouches”.  the shelf life.
 that the devices are not able to fulfil the intended use with the   •  Use packaging which are
                                                        resistant up to a temperature
 required safety level.                                 of 141°C (286°F) and in
 •  Use only clean water in all cleaning and rinsing steps.  accordance with
                                                        EN ISO 11607.
 Step-by-step procedure


 Operation  Operating mode  Warning
 •  Disassemble the
 1  Disassembling
 device.













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