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Medical Windows Tablet M101P-ME User Guide
1.5 Declaration of Conformity (DoC)
FCC Statement
This device complies with part 15 FCC rules.
Operation is subject to the following two conditions:
This device may not cause harmful interference.
This device must accept any interference
received including interference that may cause
undesired operation
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 when the equipment is operated in a commercial
environment. This equipment generates, uses, and can radiate radio frequency energy and, if
not installed and used in accordance with the instruction manual, may cause harmful
interference to radio communications. Operation of this equipment in a residential area is
likely to cause harmful interference in which case the user will be required to correct the
interference at him own expense.
CE Notice (European Union)
Medical electrical equipment Part 1-2: General requirements for
basic safety and essential performance - Collateral Standard:
Electromagnetic disturbances
EN 60601-1-2:2015
EN 5511:2019+A1:2010
EN 61000-4-2: 2009
EN 61000-3-2:2014
EN 61000-4-3: 2006+A1: 2008+A2: 2010
EN 61000-3-3:2013
EN 61000-4-4: 2012
EN 61000-4-5: 2006
EN 61000-4-6: 2014+AC:2015
EN 61000-4-8: 2012
EN 61000-4-11: 2004
Medical electrical equipment Part 1: General requirements for
basic safety and essential performance
EN 60601-1:2016/A1:2013/A12:2014
This equipment is in conformity with the requirement of the following EU legislations and
harmonized standards. Product also complies with the Council directions.
1.6 Classification
Supply Class I adapter
No applied part
IP65 (Only for panel)
Continuous Operation
Not AP or APG category
