The OsmoPRO
®
Micro-Osmometer Service Manual
• WARNING: When returning this product
for service, or shipping this product to a
second location, remove all hazardous
specimens and decontaminate the product
before packaging it for shipment. If the
product cannot be decontaminated, consult
with your shipping agent for instructions
on appropriate packaging and marking.
Hazardous Material
Cautions
• WARNING: Handle all biohazardous
materials according to established good
laboratory practices and follow your insti-
tution’s exposure control plan. Persons
handling human blood and body fluid
samples must be trained in blood-borne
hazards and observe universal precautions.
Universal precautions is an approach to
infection control under which all human
blood and body fluids are treated as if
they are known to be infectious. Use per-
sonal protective equipment
, such as
gloves, gowns, etc., to prevent exposure.
Store biohazardous materials in regulated
waste containers and dispose of these
materials in a safe and acceptable manner
that is in compliance with all country, state
and local requirements.
• If a biohazardous material is spilled on or
inside the equipment, decontaminate the
equipment using a 1% bleach solution, or
as outlined by those policies and proce-
dures established within your institution.
• To avoid injury or fire hazard, do not oper-
ate this product in an explosive atmos-
phere.
Regulatory Notices
• This product has been designed and manu-
factured in accordance with U.S.,
Canadian, and European regulatory
requirements as outlined below.
Modifications made to this product, which
are not expressly approved in writing by
the manufacturer, void the user’s authority
to operate this product, as well as any pre-
viously issued factory approvals and the
user’s rights under the warranty.
• The distributor or dealer may have applied
additional local, national, or international
approvals to this product. Consult with the
distributor or dealer to obtain further infor-
mation an/or documentation regarding
these approvals.
• Connections to this product must be made
with industry standard cables.
Symbol Conventions
This symbol indicates conformity to
relevant European directives.
This symbol indicates the product
was tested to conform to relevant
Canadian and U.S. safety standards
by Intertek Testing Services NA,
Inc. The ETL mark is approved in
the United States as a Nationally
Recognized Testing Lab (NRTL) by
OSHA, and in Canada by the
Standards Council of Canada.
In Vitro Diagnostic Medical Device
complying with EU Directive
98/79/EC.
This symbol indicates conformity to
the intent of EU Directive
2011/65/EU.
FCC Requirements
WARNING: Changes or modifications
to this unit that are not expressly
approved by Advanced Instruments
could void the user’s authority to operate
the equipment.
• This equipment has been tested and it was
found to be in compliance with the limits
for a Class B digital device, pursuant to
Part 15 of the FCC Rules. These limits
are designed to provide reasonable protec-
tion against harmful interference in a resi-
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