COMPLIANCE INFO_2023 - Laserfiche WebLink

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(i) If the design is drawn directly onto the skin,it shall be applied with a single-use article only. (j) Cabinets for the storage of instruments,dyes,pigments,and single-use articles,shall be provided for each artist and shall be maintained in a sanitary manner,which protects the instruments from contamination. (k) Needles, needle bars, grommets, and razors shall be discarded into the sharps waste container immediately upon completion of the procedure. (1) The surface of all work tables and chairs or benches shall be constructed of a material that is smooth,nonabsorbent,and easily decontaminated. (m) Worktables/trays and chairs or benches shall be decontaminated with a germicidal solution after each tattoo application. Hard surface disinfection will consist of Madacide and/or Bleach wipes All hard surfaces in the procedure area will be disinfected after each client. The chaos,counters,etc.will be sprayed with: Madacide.Caveside.and/or Bleach wipes. The disinfectant will be allowed a contact time of Between 10-15 minutes or:(according to manufachirer's directions for dilution and contact time), then wiped down with a paper towel which is disposed of in the trash. (n) All materials applied to the human skin shall be from single-use dispensers transferred from bulk containers to single- use containers and shall be disposed of after each use. (o) No animals shall be permitted in the procedure area. (2) RECORDS (a) Records,including a complete informed consent forth and post-procedure instructions for all tattoo, brand,and piercing administered, shall be maintained by the holder of the permit. All records will be maintained on-site and available for review for a period of:Two(2)Fears,after which tile records shall be shredded to destroy confidential medical information. (b) A copy of all registrations, licenses, and Exposure Control Training for all body artists employed or contracted to the facility will be maintained on-site,and available for review. (c) Records and procedure logs of all purchased pre-sterilized instruments/parts will be maintained on-site,and available for review for a period of: 90 days after the instrument is used.