N.Y. Comp. Codes R. & Regs. Tit. 10 §§ 70-5.1 - Treatment technology approval
(a) No alternative regulated medical waste
treatment system shall be used in New York State unless the Commissioner of
Health has approved the system's technology pursuant to this Subpart. The
system manufacturer, as applicant for technology approval, shall:
(1) submit an application on forms prescribed
by the Commissioner of Health;
(2)
demonstrate that the system's operation does not pose a threat to public health
or safety, including documentation that any chemical used in the system has
been registered and approved by the New York State Department of Environmental
Conservation for use in New York State;
(3) provide documentation that any chemical
used in system to treat regulated medical waste has been registered with the
Federal Environmental Protection Agency;
(4) establish the system's operating
parameters through efficacy testing, and demonstrate that the system
effectively treats regulated medical waste. Unless precluded by system design:
(i) efficacy testing shall be conducted on an
actual full-scale working model of the system, rather than a simulation, or
other substitution in scale or in kind; and
(ii) such testing shall employ surrogate test
loads, varying in organic to non-organic and solid to liquid compositions. Such
surrogate test loads shall include mycobacterium species and/or other
appropriate indicators as determined by the department, that has been
strategically placed throughout the test loads; and
(5) agree to provide all facilities in New
York State that use the alternative treatment system with a copy of the
department's technology approval letter, and any appendices or amendments
thereto for the period in which the system is in use in New York
State.
(b) Whenever
mycobacterium species is used as a biological indicator, effective treatment
shall be demonstrated by a 6 log 10 reduction in viable
cell concentrations; Bacillus atrophaeus or Geobacillus stearothermophilus are
used as a biological indicator, effective treatment shall be demonstrated a 4
log 10 reduction in viable spores concentration. No
alternative treatment system that fails to attain such reductions or fails to
demonstrate that the waste has been treated shall be used to treat regulated
medical waste.
(c) The department
may require that the system undergo supplemental efficacy testing using
organisms or agents other than those identified in subdivision (b) of this
section, and may require the manufacturer to demonstrate that the technology
meets manufacturer's claims for effective treatment of non-typical bioloads or
materials, for example, new and emerging pathogens or pathological
waste.
Notes
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