Instructions Manual

IFU-20D001-20220913
Page 26
Indicates a carrier that contains UDI information
Indicates the medical device manufacturer, as defined in the EU Regulation (EU)
2017/745.
To identify the country of manufacture of products
Indicates the Authorized representative in the European Community.
Mandatory marking for devices entering the European market to indicate conformity
with the essential health and safety requirements set out in European Regulation.
US Federal Communication Commission
Waste Electrical and Electronic Equipment Directive
Rx only
Prescription only or "For Use by or on the order of a licensed medical professional
Symbols found in the electronic camera device are not included. For iPhone user, please visit
www.apple.com to learn how to use your device. The iPhone user guides are available on the Apple
website.
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