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Amico NFPA Triplex RVL Modular Stack Mount User Manual

Page 13

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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 Standards 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 verify 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.

3.

Statement declaring that the MGEM has no fiduciary interest in the verifier and that the verifier is

not an agent or representative of the MGEM.

4.

Statement declaring that the installing contractor has no fiduciary interest in the verifier and that

the verifier has no fiduciary interest in the contractor.

C. Pre-approval

1.

Written pre-approval is required for equipment not exactly matching specifications. Submit the

information required under submittals above, attaching a cover letter stating the exact areas of

deviation.

2.

A request for preapproval of equipment must be received by the engineer no less than three days

(72 hours) prior to bid.

QUALITY ASSURANCE

A.

Regulatory Requirements

1.

Electrical Control systems and Medical Gas Alarms are to be UL listed as assemblies with

label

affixed.

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