5
Introduction
Read chapter “2 Notes for your safety” on page 15 before using the
product for the rst time. This will help you to avoid potentially danger-
ous situations.
This device bears the CE marking CE in accordance with the European
Medical Device Regulation (MDR) 2017/745.
The product complies with all applicable requirements of Directive
2011/65/EU on the restriction of the use of certain hazardous substances
in electrical and electronic equipment (“RoHS”).
The Declarations of Conformity and our General Terms and Conditions
can be viewed on our website at www.atmosmed.com
.
The quality management system at ATMOS has been certi ed according
to international standard EN ISO 13485.
These operating instructions are valid for the following devices:
• ATMOS Scope 507.7000.0
• ATMOS Scope Pro 507.7050.0
• ATMOS Scope iPrime 507.7060.0
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