App. 1
Standards and Safety
This manual contains information and warnings that must be followed to ensure safe performance of AccuScreen. Local gov-
ernment rules and regulations, if applicable, should be followed at all times.
App. 1.1
AccuScreen symbols
Symbol
Definition
Consult user manual for warnings and cautions.
Complies with Type BF requirements of IEC60601-1.
MEDICAL - General Medical Equipment as to electrical shock, fire and mechanical hazards only in accord-
ance with UL 60601-1, first edition, 2003 CAN/CSA-22.2 No. 601.1-M90.
Complies with Medical Devices Directive 93/42/EEC and RoHS Directive (2011/65/EC).
Electronic
equipment
covered
by
the
Directive
2002/96/EC
on
waste
electrical
and
electronic
equipment
(WEEE).
All
electrical
and
electronic
products,
batteries,
and
accumulators
must
be
taken
to
separate
collection
at
the
end
of
their
working
life.
This
requirement
applies
in
the
European
Union.
Do
not
dispose
of
these
products
as
unsorted
municipal
waste.
You
can
return
your
device
and
accessories
to
Natus Medical Denmark A/S
,
or
to
any
Natus Medical
Denmark A/S
supplier.
You
can
also
con-tact
your
local
authorities
for
advice
on
disposal.
App. 1.2
Accessory symbols
Symbol
Definition
Non sterile product.
Do not reuse.
88
Otometrics - MADSEN AccuScreen
App. 1 Standards and Safety
