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iv
User manual OR 100 /110, ed. 5
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 Di-
agnostics 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 re-
quirements. Such products are labelled with the "crossed out wheelie", de-
picted 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 manufac-
turer will take care of the proper disposal and recycling of the instru-
ment 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 collec-
tion & 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
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