Page 71 - Abbott

Symbol Description
Consult instructions for use

Keep dry

Date of Manufacture

Manufacturer

Temperature limitations

Humidity limitation

Serial number

Made in USA

Momentary pushbutton

Quantity, package contents

Do not use if package is damaged

The device contains a battery and the label is affixed to this device in accordance with European Council
Directives 2002/96/EC and 2006/66/EC.

These directives call for separate collection and disposal of electrical and electronic equipment and
batteries. Sorting such waste and removing it from other forms of waste lessens the contribution of
potentially toxic substances into municipal disposal systems and into the larger ecosystem.

Return the device to St. Jude Medical at the end of its operating life.
Direct current

Federal Communication Commission Number (FCC ID: #)

Non-ionizing radiation

Type BF Patient Applied Part

IEC 60529 Ingress Protection Level

Class II equipment

Manufacturing Facility

Australian Communications and Media Authority (ACMA) and New Zealand Radio Spectrum Management
(RSM) Regulatory Compliance Mark (RCM)

For prescription use only

Conforms to
AAMI Std ES60601-1
Certified to CAN/CSA std C22.2 No. 60601-1

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