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ESD sensitivity
Manufacture date
Serial number
European community representative
This mark means that this device is fully in conformance with the
Council Directive Concerning Medical Devices 93/42/EEC. The
number adjacent to the CE marking (0123) is the number of the
EU-notified body that certified meeting the requirements of Annex
II of the Directive.
The following definition of the WEEE label applies to EU member
states only.
This symbol indicates that this product should not be treated as
household waste. By ensuring that this product is disposed of
correctly, you will help prevent bringing potential negative
consequences to the environment and human health. For more
detailed information with regard to returning and recycling this
product, please consult the distributor from whom you purchased it.
* For system products, this label may be attached to the main unit
only.
Classified by Underwriters Laboratories Inc. with respect to electric
shock, fire and mechanical hazards, only in accordance with UL
60601-1, CAN/CSA C22.2 NO.601-1, IEC 60601-1-1, IEC
60601-2-27, IEC 60601-2-30, IEC 60601-2-34, IEC 60601-2-49.
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