2.1.4
Identical Products
Products of the same classification shall be identical. This requirement
includes all component equipment, modules, assemblies, parts, and materials.
2.1.5
Nameplates and Equipment Markings
a. Each major equipment component shall have the Manufacturer's name,
model, and serial number on a plate secured to the equipment. Also, all
compliance with regulatory requirements, such as UL and CFR, shall be
indicated on the nameplate or on adjacent labels.
b. All controls on call stations shall be plainly and permanently labeled
with the identification of the function served. Stick on marker tapes is
not acceptable.
c. Markings on any exposed surfaces shall not be destroyed by housekeeping
solutions normally used in medical facilities.
2.1.6
Mounting Alignment Capability
Wall mounted components shall have an adjustable mounting alignment
capability to compensate for improperly aligned backboxes and to insure a
plumb, square, and level installation.
2.1.7
Model and Enhancements
a. The system and all product components shall be the Manufacturer's
latest model, design, version, and quality in production at time of
delivery and installation.
b. Any product hardware or software enhancement that becomes available
after delivery and installation, and up to time of system acceptance, shall
be brought to the attention of the Contracting Officer upon announcement by
the Manufacturer and shall be made available to the medical facility. If
such enhancements customarily are provided at no additional cost, the
Government shall automatically be entitled to such enhancements. If such
enhancements customarily are provided at additional cost, the Contracting
Officer has the option to accept or reject such enhancements.
c. Submit a letter to the Contracting Officer from the Manufacturer
guaranteeing that the Manufacturer shall inform the Government of, and make
available to the Government, all commercially available enhancements to the
system hardware or software at the then current price. Include the letter
with the product data submittal.
d. Substitutions, modifications, or improvements to a system hardware and
software are permissible provided that such substitution, modifications, or
improvements shall not reduce or degrade the performance or product
requirements, nor violate regulatory requirements. No such substitutions,
modifications, or improvements shall be made without the written consent of
the Manufacturer and Contracting Officer. Such consent shall not be
unreasonably withheld or delayed.
2.1.8
Software and License
a. Provide all software required for the specified capability,
configuration, performance, and operation of the system.
SECTION 16731A
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