Advanced Instruments Anoxomat III Service Guide

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Anoxomat® III ServiceGuide
Appendix B
Regulatory notices
This product has been designed and manufactured to meet the intent of 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 documentation.
Connections to this product must be made with industry-standard cables. Use of non-shielded cables may violate RFI/EMI
limits.
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.
This symbol indicates the product conforms to the requirements of EU
Directive 2012/19/EU on “Waste Electrical and Electronic Equipment”
when disposed of in accordance with the provisions of Appendix C.
IVD
In Vitro Diagnostic device in US and Canada. In EU, complies with
2014/30/EU and 2014/35/EU as General Laboratory Use product.

Advanced Instruments Anoxomat III Specifications

General

Brand	Advanced Instruments
Model	Anoxomat III
Category	Medical Equipment
Language	English