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© Guldmann GB/US-04/2023 • # 561577_102
© Guldmann GB/US-04/2023 • # 561577_102
15.00 EU-Declaration of conformity
The product is manufactured in compliance with regulation (EU) 2017/745
of the European parliament and of the Council of 5 April 2017, as medical
device Class I.
16.00 Environmental policy statement - V. Guldmann A/S
Guldmann is continuously working towards ensuring that the company’s
impact on the environment, locally and globally, is reduced to a minimum.
It is Guldmann’s goal to:
• Comply with the current environmental legislation (e.g. WEEE and REACH
directives)
• Ensure that we, at the widest possible range, use RoHS compliant materials
and components
• Ensure that our products do not have an unnecessary negative impact on the
environment regarding use, recirculation or disposal
• Ensure that our products contribute to a positive working environment in the
places they are utilised
Inspections are made annually by the Department for Nature and Environ-
ment from the Municipality of Aarhus using the Danish Environmental Protec-
tion Act, section 42 as a reference.
17.00 EMC Information
Tabel 1
Guidance and manufacturer’s declaration – electromagnetic emissions
The GL5.2 is intended for use in the electromagnetic environment specied below.
The customer or the user of the GL5.2 should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1 The GL5.2 uses RF energy only for its internal function. There-
fore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Class A The GL5.2 is suitable for use in all establishments, including do-
mestic establishments and those directly connected to the public
low-voltage power supply network that supplies buildings used
for domestic purposes.
Voltage uctuations/
icker emissions
IEC 61000-3-3
Complies
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