15. Product Disposal
Dispose of the device in accordance with all local and government laws
and regulations. For more information, contact the local authority
responsible for waste disposal.
16. Signs and Symbols
This device complies with the essential requirements of Directive 93/42/
EEC for medical devices.
This equipment has been tested and found to comply with the limits for a
Class B digital device, pursuant to part 15 of the FCC Rules.
Applied Part, Type BF
for Medical Electrical Equipment - EN 60601-1
IP22
Protected from touch by fingers and objects greater than 12 millimeters.
Protected from water spray less than 15 degrees from vertical.
Direct current (DC) power supply
Do not dispose this product as unsorted municipal waste. Dispose of in
accordance to local regulations. Directive 2002/96/EC (WEEE)
Device serial number, uniquely identifies each manufactured unit.
Lot code or batch code.
Date of manufacture, represented as a date code.
Manufacturer contact information.
European representative for the manufacturer.
Catalog or model number - ISO 15223-1:2016
Caution
Follow instructions before use.
17. Regulatory Compliance
17.1. FCC Information - Compliance with FCC Rules, Part 15
This equipment has been tested and found to comply with the limits for a Class
B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed
to provide reasonable protection against harmful interference in a residential
installation. This equipment generates, uses, and can radiate radio frequency
energy and, if not installed and used in accordance with the instructions, may cause
harmful interference to radio communications. However, there is no guarantee
that interference will not occur in a particular installation. If this equipment
does cause harmful interference to radio or television reception, which can be
determined by turning the equipment off and on, the user is encouraged to try to
correct the interference by one or more of the following measures:
16
0598