Leica Aperio GT 450 DX User Manual page 9

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Aperio GT 450 DX User's Guide, Revision B © Leica Biosystems Imaging, Inc. 2022
Regulation/
Description
Standard
Medical Devices
Device is in compliance with UK Conformity Assessment requirements.
Regulations 2002
ISO 15223-1 - 5.4.4 Caution
SO 7010 – W001 General warning
TÜV Product Services have certified that the listed products comply with both
IEC 61010-1
U.S. and Canadian safety requirements.
IEC 60417 - 5031 This device is suitable for direct current only.
On. To indicate connection to the mains, at least for mains switches or their
IEC 60417 - 5007
positions, and those cases where safety is involved.
Off. To indicate disconnection from the mains, at least for mains switches, and
IEC 60417 - 5008
all those cases where safety is involved.
ISO 15523-1 5.7.3 Temperature limitation
ISO 15223-1 5.3.8 Humidity limitation
Device is regulated under 2012/19/EU (WEEE Directive) for Electrical and
2012/19/EU
Electronic Equipment Waste and must be discarded under special conditions.
People's Republic Device contains certain toxic or hazardous elements and can be used safely
of China Electronic during its environmental protection use period. The number in the middle of
Industry Standard SJ/ the logo indicates the environmental protection use period (in years) for the
T11364 product. The outer circle indicates that this product can be recycled.
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