Information On Labelling And Safety; Laws And Provisions Related To The Product - HEINE EN200 BP Mode D'emploi

•
Defects due to material or production faults are removed free of charge within
the warranty period.
•
A warranty claim does not result in an extension of the warranty period, either
for the device or for the replaced component.
•
The following are excluded from any warranty claim:
a. all damage caused as a result of incorrect handling, e.g. due to non-
compliance with the instructions for use.
b. damage due to repairs or interventions by the buyer or unauthorized third
parties.
c. transport damage that occurs en-route from the manufacturer to the user or
if it is sent to the service centre.
d. accessories that are subject to normal wear, such as batteries, cuffs, etc.
•
No liability for direct or indirect consequential damages caused by the device
is accepted if the damage to the device is identified as a warranty case.
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INFORMATION ON LABELLING AND SAFETY

LAWS AND PROVISIONS RELATED TO THE PRODUCT

This device is designed in accordance with Medical Device Directive 93/42/EEC,
Class IIa, and corresponds to protection class II. type BF pursuant to
DIN EN 60601-1
DIN EN 60601-1:2013-12
General requirements for basic safety and essential performance
DIN EN 80601-2-30:2011-05
Particular requirements for the basic safety and essential performance of automated
type non-invasive sphygmomanometers
DIN EN 60601-1-2:2007-12
Electromagnetic compatibility: the device complies with the standard's requirements
for electromagnetic compatibility.
Other provisions: The accident prevention measures, provisions and requirements
in the respective user's country apply for users outside the Federal Republic of
Germany.
MED 113275 2018-02-26
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