biodex 950-192, Руководство по эксплуатации

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Biodex Medical Systems, Inc. © 2018
Product Certifications and Classifications
The medBike has received the following certifications, and falls within the following
classifications:
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EN: ISO 20957-1:2013.
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UL: 1647:2011/R2014-11.
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CAN/CSA-C22.2 No.68: 2009 + UPD No. 1:2010-02 + UPD No. 2: 2010 + 09.
FCC: Compliance:
•
EN55014-1: 2006 / A2: 2011.
•
EN55014-2: 1997 / A2: 2008.
•
EN61000-3-2: 2014.
•
EN61000-3-3:2013.
NOTE: Circuit diagrams for this product are provided on the Biodex website,
www.biodex.com or can be obtained by contacting Biodex Customer Service (see
Contact information).
Note: Complete information on the Electromagnetic Compatibility for the medBike can be
located in the Compliance Supplement located on the Biodex website (www.biodex.com) or can
be obtained by contacting Biodex Customer Service (see Contact information).
Before Proceeding
NOTE: The warnings, cautions and instructions provided in this manual must be
read, followed and kept available for consultation at all times. Observing the
information, instructions, and procedures presented throughout this manual is
essential for using this product both properly and safely.
SPECIFIC CAUTIONS
●
Allow only qualified, trained personnel to operate or service this product.
●
If the equipment is used in a manner other than specified in this operation
manual, the protection provided by the equipment may be impaired and
results could be compromised.
CAUTION: Unauthorized modifications to this product are not permitted and will
void the manufacturer’s warranty. Unauthorized modification of the product may
result in a hazard to the user and/or patient. Do not modify this equipment
without authorization from the manufacturer.
For additional technical advice, service or education information, please contact: