App.
60
Specifications
MAJ-2301 INSTRUCTION MANUAL
Medical Devices Directive
This device complies with the requirements of Directive 93/42/EEC
concerning medical devices.
Classification: Class
I
RoHS Directive
This device complies with the requirements of Directive
2011/65/EU concerning electrical and electronic equipment.
RE Directive
This device complies with the requirements of DIRECTIVE
2014/53/EU OF THE EUROPEAN PARLIAMENT AND OF THE
COUNCIL of 16 April 2014 (RED).
WEEE Directive
In accordance with European Directive 2002/96/EC on Waste
Electrical and Electronic Equipment, this symbol indicates that the
product must not be disposed of as unsorted municipal waste, but
should be collected separately.
Refer to your local Olympus distributor for return and/or collection
systems available in your country.
EMC
Applicable standard
IEC 60601-1-2:2014
• Compliant to the EMC requirements for medical equipment
edition 4 (IEC 60601-1-2: 2014).
• Classification by emission standard CISPR 11
Group 1, Class A
Year of manufacture
The last digit of the year of manufacture is the second digit of the
serial number. In this example, the year is 2017.
Ex. 1701234 (serial number)
