3
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HEALTH AND SAFETY
INFORMATION
Device Safety Compliance
The 3M™ Attest™ Mini Auto-reader 490M complies with the following standards as
demonstrated by the CB Scheme Certificate and test report issued by UL, LLC (UL):
• IEC/EN 61010-1:2010� Safety requirements for electrical equipment for
measurement, control, and laboratory use - Part 1: General requirements
• IEC/EN 61010-2-010:2014� Safety requirements for electrical equipment for
measurement, control, and laboratory use - Part 2-010: Particular requirements
for laboratory equipment for the heating of materials�
The 3M™ Attest™ Mini Auto-reader 490M is UL Listed and carries the UL mark with
adjacent indicators “C” and “US” based on compliance to the standards UL 61010-1,
CAN/CSA 22�2 No� 61010-1 and CAN/CSA 22�2 No� 61010-2-010�
The 3M™ Attest™ Mini Auto-reader 490M complies with the CE mark related to
the Low Voltage Directive (LVD) 2014/35/EU as confirmed in the Declaration of
Conformity�
The 3M™ Attest™ Mini Auto-reader 490M complies with the RoHS Directive,
Directive 2011/65/EU of the European Parliament and of the Council of 8 June
2011 on the restriction of the use of certain hazardous substances in electrical and
electronic equipment�
The 3M™ Attest™ Mini Auto-reader 490M complies with China RoHS
II requirements�
The 3M™ Attest™ Mini Auto-reader 490M complies with the WEEE Directive,
Directive 2012/19/EU of the European Parliament and of the Council of 04 July
2012 on waste electrical and electronic equipment (WEEE)�
EMC Compliance
The 3M™ Attest™ Mini Auto-reader 490M complies with the following EMC
standards as confirmed in the Declaration of Conformity generated by 3M:
• IEC 61326-1:2012/EN 61326:2013 Electrical equipment for measurement, control
and laboratory use - EMC requirements - Part 1: General requirements
• EMC requirements of the CE mark EMC Directive 2014/30/EU�
The 3M™ Attest™ Mini Auto-reader 490M complies with the Australian and
New Zealand electrical safety and electromagnetic compatibility requirements as
confirmed in the Supplier’s Declaration of Conformity that is linked to the Australian/
New Zealand Regulatory Compliance Mark (RCM)�
CAN ICES‑3 (B)/NMB‑3(B)
This device complies with part 15 of the FCC Rules� Operation is subject to the
following two conditions: (1) This device may not cause harmful interference, and (2)
this device must accept any interference received, including interference that may
cause undesired operation�
Modifications to this device shall not be made without the written consent of 3M
Company� Unauthorized modifications may void the authority granted under Federal
Communication Rules permitting the operation of this device�
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 in a residential
installation� This equipment generates, uses and can radiate radio frequency energy
and, if not installed and used in accordance with the instructions, may cause
harmful interference to radio communications� However, there is no guarantee that
interference will not occur in a particular installation� If this equipment does cause
harmful interference to radio or television reception, which can be determined
by turning the equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
- Reorient or relocate the receiving antenna�
- Increase the separation between the equipment and receiver�
- Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected�
- Consult the dealer or an experienced radio/TV technician for help�
EXPLANATION OF PRODUCT
AND PACKAGING LABEL SYMBOLS
Symbol Glossary
Symbol Title
Symbol
Description and Reference
Manufacturer
Indicates the medical device
manufacturer as defined in Medical
Device Regulation (EU) 2017/745
formerly EU Directive 93/42/EEC�
Source: ISO 15223, 5�1�1
Authorized
Representative in
European Community
Indicates the authorized representative
in the European Community� Source:
ISO 15223, 5�1�2, 2014/35/EU, and/or
2014/30/EU
Date of Manufacture
Indicates the date when the medical
device was manufactured� Source: ISO
15223, 5�1�3
Catalogue number
Indicates the manufacturer's catalogue
number so that the medical device can
be identified� Source : ISO 15223, 5�1�6
Serial number
Indicates the manufacturer's serial
number so that a specific medical
device can be identified� Source: ISO
15223, 5�1 �7
Caution
Indicates the need for the user to
consult the instructions for use for
important cautionary information
such as warnings and precautions that
cannot, for a variety of reasons, be
presented on the medical device itself�
Source: ISO 15223, 5�4�4
CE Mark
Indicates conformity to all applicable
European Union Medical Device
Regulations and Directives�
UL Listed
Indicates product was evaluated and
Listed by UL for the USA and Canada�
Regulatory Compliance
Mark
Indicates product complies with
applicable Australian regulatory
requirements� Source: AS/NZS
4417�1:2012
China RoHS II symbol
Indicates the product’s environmental-
friendly use period in years� Source:
SJ/T 11364-2014
Direct current
To indicate on the rating plate that the
equipment is suitable for direct current
only or to identify relevant terminals�
Source: IEC 60417-5031
Recycle electronic
equipment
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)
For more information see, HCBGregulatory.3M.com
