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` �N�� <br /> ~ ` ~Only equipmnentmanu�x�unadfo���sterilization ofmedical instruments shall b~=�used. <br /> •Gbari|bnationaguipmentmhaUbebaobaduminAecommencio|biokoxicali/dkcadormonKohngeystem <br /> after the initial installation, after any major repair,and etleast once permnonth.Theooqpination <br /> date ofthe monitor shall bechecked prior bmeach use. ' <br /> °Each sterilization load shall bemonitored with mechanicalindicators for time,temperature, <br /> pressure, and, at a minimum, Class V integrators. The Class V integrator gives an immediate <br /> response on whether the sterilization has been achieved. Each individual sterilization pack <br /> shall have an indicator. <br /> • Biological indicator monitoring test results shall borecorded|nm log thatshall bmkept onsite for <br /> two years after the date ofthe results. / <br /> °Awritten log ofeach sterilization cycle shall be retained on site for two years and shall include all <br /> ofthe following information: '| <br /> / <br /> The date ofthe load. � <br /> (b)A list ofthe contents ofthe load. ` | <br /> (c)The exposure time and temperature. � <br /> (d)The results ofthe Class Vintegrator. ! <br /> (e)For cycles where the results ofthe biological indicator monitoring temtmnapomitiva howthe�*n�mvmenaokaoned. andpnoofofanegpd� � <br /> negative test ' <br /> 3. Clean instruments and sterilized instrument packs shall bmplaced in <br /> ' labeled— containers,^ <br /> ormtonedina|obe|eduobinettbathopnzbechadfnmmduotendmmkstunm.� W clean gloves to handle <br /> sterilized packages to prevent cross contamination of the sterilized item when the package is opened <br /> for use. <br /> 4. S0odtzed instruments shall bestored inthe intact orin ' steh|izetionmqu�n�ent <br /> � <br /> n� hdgeunt bn�eofuse. <br /> equipment <br /> 5. Sterile instrument packs shall ie evaluated at the time of <br /> apockkacmnmpnom/iaed. inc(uding. budnotUnnhedbzcommovvhene~ ���� - ' <br /> d�p|a�ngany ejdenoeofmohtmneconbanminatkm 0heponkmho||-- '�–�--''^''~''~�'�"' "��' °' <br /> . weu"�cp,ueoorreprocessed <br /> before use. <br /> ' –' <br /> / <br /> Ei A body art facility that does not afford access to a decontamination and sterilization area that <br /> meets the standards of subdivision(c)of Section 119314 of the California Health and Safety Code or <br /> that does not have sterilization equipment shall use only purchased disposable,single-use, pre- <br /> sterilized instruments. In place of the requirements for maintaining sterilization records,the following <br /> records shall be kept and maintained for a minimum of 90 days following the use of the instruments at <br /> the site of practice for the purpose of verifying the use of disposable,single-use,pre-sterilized <br /> ~Krecord ofpurchase and use ofall single-use instruments. ' <br /> °Alog ofall procedures, including the names ofthe practitioner and client <br /> ' andthe date ofthe <br /> procedure. <br /> / <br /> OPERATING CONDITIONS FOR AUTOCLAVE <br /> Cleaning: Remove all material onthe instruments during the -- �----' toensure that the <br /> sterilization process|aachieved. The cleaning process can be -manual–cleaning orbyuse ofan <br /> ultrasonic machine. — <br /> Packaging: Package the instruments with hinges inthe open to ensure <br /> cne/�eoofthe inatuunnem�are a��|�ad. -----' ---- <br />