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This product has been designed and manufactured in accor-
dance 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 distributor or dealer for more information and documen-
tation.
•
Connections to this product must be made with shielded
cables. Use of non-shielded cables may violate RFI/EMI
limits.
Symbol Conventions
This symbol indicates conformity to relevant European direc-
tives.
This symbol indicates the product was tested to conform to rele-
vant 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.
Regulatory Notices
Appendix C
Содержание 3900
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