Utah Admin. Code R392-701-10 - Disinfection and Sterilization Requirements
(1) The operator shall ensure that:
(a) any item or instrument used for body art
that is contaminated during the procedure is immediately replaced with a
sterilized instrument or item before the procedure resumes;
(b) any reusable item or instrument that may
have been exposed to bloodborne pathogen contamination during a body art
procedure is sterilized before use;
(c) at the conclusion of each client service,
multi-use implements, such as a tattoo machine, and other tools which cannot be
sterilized in an autoclave or immersed in liquid without being damaged are
cleaned and disinfected in the following sequential manner:
(i) remove visible debris;
(ii) disinfect with a chemical disinfectant
spray or wipe according to the manufacturer's directions; and
(iii) store covered in a clean, dry
location;
(d)
disinfection is carried out using a chemical disinfectant in accordance with
the manufacturer's directions;
(e)
each instrument used for a body art procedure remains stored:
(i) in a sterile package until just before a
body art procedure; or
(ii) cleanly
in a container, ready for sterilization immediately before the
procedure;
(f) except as
specified in Subsection (1)(c), reusable body art instruments are packed
individually in sterilization packaging and subsequently sterilized in the
autoclave described in Subsections R392-701-7(1)(c)(i) through (iii) after
being cleaned as specified in Subsection (1)(g);
(g) except as specified in Subsection (1)(c),
reusable body art instruments are processed after each use in the processing
area according to the following sequential order:
(i) soak in an enzymatic cleaning
solution;
(ii) scrub to remove
visible debris;
(iii) rinse and
inspect for visible debris;
(iv)
process through an ultrasonic cycle or automated instrument washer;
(v) rinse;
(vi) air dry; and
(vii) inspect for any remaining residue or
debris;
(h) floors,
walls, ceilings, tables, counters, shelves, furniture, furnishings, and
plumbing fixtures are kept clean and in good repair;
(i) packages, sterile equipment, and body art
materials are not used without first being reprocessed and sterilizing again if
the package, equipment, or material:
(i) has
been visibly compromised; or
(ii)
has not been stored as required in Subsection (1)(e);
(j) reusable body art instruments are
transported from the procedure area to the processing area in a container with
a secured lid;
(k) reusable body
art instruments remain stored in sterile packages or other containers designed
for sterilizing instruments that are marked with the sterilization date until
just before they are used for a body art procedure;
(l) sterilization packaging contains either
an internal temperature sterilization indicator or Class 5 steam sterilization
integrator;
(m) tables, counters,
chairs, floors, and other work surfaces are cleaned and disinfected after each
use regardless of whether contamination is visible;
(n) the date of sterilization and cycle
number is noted on the sterilization packaging; and
(o) when utilizing on-demand sterilization in
which an instrument or material is placed into an autoclave to be sterilized
immediately before the body art procedure, the sterilization cassette contains
an internal temperature sterilization indicator or steam sterilization
integrator.
(2)
Single-use items may be packed in peel-packs with a clean, reusable instrument
before being sterilized provided they are arranged in a manner that will allow
each item to be properly sterilized.
(3)
(a) The
operator shall conduct spore testing, according to the manufacturer's
directions, at least monthly to ensure that the sterilization equipment is
capable of attaining sterilization.
(b) These tests shall be verified through an
independent laboratory.
Notes
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