Classification, Manufacturer Symbols And Fcc Notice - SoClean 2 Manual Del Usuario

CLASSIFICATION, MANUFACTURER, SYMBOLS AND FCC NOTICE
Classification
US FDA Class I according to 21 CFR § 880.6890 - General purpose disinfectants.
EC/EU MDD Class IIa according to 93/42/EEC Annex IX Rule 15 - Device is intended to disinfect medical devices.
Designed by and manufactured for: SoClean, Inc., 12 Vose Farm Road, Peterborough, New Hampshire 03458 USA
Symbols
Authorised
representative
EC REP
in the European
Community
Consult
manual
Catalogue
number
FCC Notice
Please note that changes or modifications not expressly approved by the party responsible for compliance
could void the user's authority to operate the equipment.
NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 18 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:
• Reorientate or relocate the receiving aerial.
• Increase the separation between the equipment and the receiver.
• Connect equipment into an outlet on a circuit different from that to which the receiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.
Manufacturer
JDI Electronics Factory
Sima Industrial Zone, Sima Village, Changping Town,
Dongguan City, Guangdong Province, China 523570
Waste Electrical and Electronic Equipment (WEEE).
It is the responsibility of the end user to dispose
of this equipment at a designated collection point.
Not made with
natural rubber latex
Complies with
Medical Device
Directive of the
0120
European Union.
Serial number
Date of
manufacture
Do not use
if package
is damaged.
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