Amico NFPA Triplex SCD Modular Stack Mount - Manual (Page 14)

Amico Source Equipment 12
vi. Air filters including type and replacement element.
vii. Pressure regulators including type and manufacturer.
viii. Dew point monitor including technology employed, calibration interval, and annual
drift in degrees.
ix. Carbon monoxide monitor including technology employed, calibration interval,
and annual drift in ppm.
x. Air dryers, type, manufacturer, and design dew point at least -40˚F (-40˚C) at 100
psig (689 kPa).
xi. Sound pressure in dB (A) when operated within the capacity as stated in the NFPA 99.
xii. Heat output (BTU) for the equipment.
c. For other medical gas products include:
i. Outlet keying system.
ii. Alarms networking instructions.
d. Complete installation instructions for the use of the installer.
e. Statement of specific compliance with paragraphs of NFPA 99 most recent edition as
relevant to the equipment and as listed in those sections.
f. Complete maintenance schedules.
g. Warranty statement which must encompass all system components. Warranties covering
only specific components or containing exclusions are not acceptable.
h. Name and contact information for installation assistance, start up, warranty and service.
i. Description of available Preventative Maintenance Programs for Owners review.
j. Information on training programs available to maintenance personnel for Owners review.
B. Medical Gas Verifier Submittals shall include:
1. Name, contact information, and reference list. Reference list should include no less than three
references on projects of similar size and complexity.
2. A notarized confirmation from the verifier stating that the verifier undertakes to validate this project
and thus agrees to disqualify themselves from supplying any equipment which will be included in
the scope of their verification. No verifier who supplies equipment shall be permitted to verify that
equipment.