The following standards were applied:
Health &
The conformity assessment procedure referred to in Article 10.4 and Annex III of Directive 1999/5/EC has been followed.
This device also conforms to the EMC requirements of the Medical Devices Directive 93/42/EEC.
Note This equipment is intended to be used in all EU and EFTA countries. Outdoor use may be restricted to certain frequencies and/or may require a license for operation. For more details, contact Cisco Corporate Compliance.
The product carries the CE Mark:
Declaration of Conformity for RF Exposure
This section contains information on compliance with guidelines related to RF exposure.
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