Section 6: Specifications - 3M Ranger 245 Bedienungsanleitung

Type BF applied part
Equipotentiality
Refer to instruction manual/
booklet
Fuse
Importer
Keep dry
Manufacturer
Medical Device
Protective earth (ground)
Recycle electronic
equipment
Rx Only
Serial number
UL Classified
Unique device identifier
For more information see HCBGregulatory.3M.com

Section 6: Specifications

Guidance and manufacturer's declaration – electromagnetic emissions
The model 245 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 245 should assure that it is
used in such an environment.
Emissions test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
Flicker emissions
IEC 61000-3-3
Guidance and manufacturer's declaration – electromagnetic immunity
The model 245 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 245 should assure that it is
used in such an environment.
Immunity Test
Electrostatic discharge (ESD)
IEC 61000-4-2
Electrical fast transient/burst
IEC 61000-4-4
To identify a type BF applied part complying with IEC 60601-1. Source: IEC 60417-5333
To identify the terminals which, when connected together, bring the various parts of an equipment or of a
system to the same potential, not necessarily being the earth (ground) potential. Source: IEC 60417-5021
To signify that the instruction manual/booklet must be read. Source: ISO 7010-M002
Indicates a replaceable fuse
Indicates the entity importing the medical device into the locale. Source: ISO 15223, 5.1.8
Indicates a medical device that needs to be protected from moisture. Source: ISO 15223, 5.3.4
Indicates the medical device manufacturer. Source: ISO 15223, 5.1.1
Indicates the item is a medical device. Source: ISO 15223, 5.7.7
To identify any terminal which is intended for connection to an external conductor for protection against
electric shock in case of a fault, or the terminal of a protective earth (ground) electrode. Source: IEC
60417, 5019
DO NOT throw this unit into a municipal trash bin when this unit has reached the end of its lifetime.
Please recycle. Source: Directive 2012/19/EC on waste electrical and electronic equipment (WEEE)
Indicates that U.S. Federal Law restricts this device to sale by or on the order of physician. 21 Code of
Federal Regulations (CFR) sec. 801.109(b)(1)
Indicates the manufacturer's serial number so that a specific medical device can be identified. Source:
ISO 15223, 5.1.7
Indicates product was evaluated and Listed by UL for the USA and Canada.
Indicates a carrier that contains Unique Device Identifier information. Source: ISO 15223, 5.7.10
Compliance Electromagnetic environment - guidance
Group 1 The model 245 uses RF energy only for its internal function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby electronic equipment.
Class B The model 245 is suitable for use in all establishments, including domestic establishments and those
directly connected to the public low-voltage power supply network that supplies buildings used for
domestic purposes.
Class A
Complies
IEC 60601 test level Compliance level
±8 kV contact ±8 kV contact
±15 kV air ±15 kV air
2± kV power lines 2± kV power lines
Electromagnetic environment - guidance
Floors should be wood, concrete or ceramic tile. If floors are covered with
synthetic material, the relative humidity should be at least 30%.
Mains power quality should be that of a typical commercial or hospital
environment.
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