2 DECADE user manual, edition 9
Intended use
For research purposes only. While clinical applications may be shown, this
instrument is not tested by the manufacturer to comply with the In Vitro
Diagnostics Directive.
WEEE directive
All equipment of Antec Leyden which are subjected to the WEEE directive
shipped after August 13, 2005 are compliant with the WEEE marking
requirements. Such products are labelled with the “crossed out wheelie”,
depicted on the left site.
The symbol on the product indicates that the product must not be
disposed as unsorted municipality waste.
Collection & recycling information
Please ship the instrument back to the manufacturer (Antec Leyden, the
Netherlands) at the end-of-life time of the product. The manufacturer
will take care of the proper disposal and recycling of the instrument at
its facilities.
Shipping address for the end-of-life products:
Antec Leyden
Industrieweg 12
2382NV Zoeterwoude
The Netherlands
In case of questions, or if further information is required about the collection &
recycling procedure, please contact your local distributor.
ROHS directive
Our instruments are currently exempt from the RoHS directive because they
fall under WEEE Annex IA categories 8 and 9, which includes medical
devices and monitoring and control instruments. Nevertheless, we have taken
steps to eliminate all restricted substances from our products.
Antec Leyden is an ISO 9001:2000 certified company.
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