About Regulatory Symbols
Medical Device Manufacturer—Indicates the name and address of the
medical device manufacturer.
Authorized European Representative — Indicates the name and address of
the legal entity designated by eSight Corporation to represent them in the
European Union.
CE Mark — This mark indicates that eSight complies with applicable
European Union regulations.
Medical Device — Indicates eSight is a medical device.
Caution — Consult the instructions for use for important information, such
as warnings and cautions.
Consult the Instructions for Use — Indicates users must read the
Instructions for Use prior to using eSight.
eIFU Indicator — Indicates that Instructions for Use are available in
electronic format on the eSight Corporation website at the stated URL.
FCC Mark — This mark certies that the electromagnetic interference
from eSight is under the limits approved by the Federal Communications
Commission.
WEEE Mark — This mark indicates that electrical and electronic equipment
must not be disposed of with ordinary household waste. See ‘Correct
Disposal’ in the Regulatory Notices section of this guide.
Recyclable — The product packaging is recyclable.
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