Olympus BF-UC180F - Page 27

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Chapter 2 Instrument Nomenclature and Specifications
ULTRASONIC BRONCHOFIBERVIDEOSCOPE BF-UC180F
Medical Devices
Directive
This device complies with the
requirements of Directive 93/42/EEC
concerning medical devices.
Classification: Class II a
RoHS
Directive
This device complies with the
requirements of Directive
2011/65/EU concerning electrical
and electronic equipment.
EMC Applied standards;
IEC 60601-1-2: 2001
IEC 60601-2-37: 2001
This instrument complies with the
standards listed in the left column.
CISPR 11 of emission:
Group 1, Class B
This instrument complies with the
EMC standard for medical electrical
equipment; edition 2 (IEC 60601-1-2:
2001). However, when connecting to
an instrument that complies with the
EMC standard for medical electrical
equipment; edition 1 (IEC 60601-1-2:
1993), the whole system complies
with edition 1.
Year of manufacture
The last digit of the year of
manufacture is given in the second
digit of the serial number.
Degree of protection
against electric
shock
TYPE BF applied part
Ingress protection
rating
IPX7 This instrument complies with the
standards for medical electrical
equipment: IEC 60601-1: 1988
IEC 60601-2-37: 2001.
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