Advanced Bilirubin Stat-Analyzer BR2, Service Manual, Page: 11 / 69

The Advanced® Model BR2 Service Manual
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, where all human blood
and body fluids are treated as if known to
be infectious. Use personal 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 require-
ments.
• 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 that are
not expressly approved in writing by the
manufacturer will void the user’s authority
to operate this product, previously 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 the dis-
tributor or dealer for more information and
documentation.
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.
11