|
Atlanta, GA
September, 2005
— North American
Medical Corporation
has successfully
completed an
independent,
third-party
engineering and
product safety
testing process
under UL's
(Underwriters
Laboratories' ®)
Certificate Services
making their
flagship spinal
treatment device one
of the only systems
in the marketplace
proven to perform
within demanding
hospital emissions
standards.
The medical device
safety testing and
engineering audit
provides
certification to
manufacturing
facilities that
demonstrate advanced
engineering, sound
scientific practices
and superior product
testing performance.
The purpose of the
certification is to
ensure end users
that an equipment
manufacturer is
committed to the
quality and safety
of the products they
provide.
”UL’s laboratory
testing program is
an extensive and
arduous process that
demands a
significant
commitment, in both
time and financial
expense,” said
Chello Grace, COO
North American
Medical. “However
given the level of
responsibility of
being in the
healthcare industry,
I just don’t see how
any manufacturer
could fail to pursue
this type of third
party certification.
An independent
certification
assures the buyer
that the product
quality and
effectiveness will
maintain full
integrity under even
the most rigorous
and extenuating
circumstances
imaginable. ”
Carlos Becerra, CEO
of North American
Medical, says that
this prestigious
certification
provides yet another
clearly significant
distinction for the
spinal treatment
systems
manufacturer. “With
continual new
patents under issue
from the U.S. Patent
Office, we have led
the industry from
the onset with
advanced and
innovative
engineering.
Competitors may try
to copy our ideas,
but they cannot copy
the quality. This
certification only
further validates
our technology and
the sound
engineering behind
it”. |
