IFU EN T800, Rev 09/2016-07-07, art.no. 8004007
3
4.
This product is not considered to be defective in materials nor workmanship by reason
that it requires adaptation in order to conform to national or local technical or safety
standards in force in any country other than the one for which the product was originally
designed and manufactured. This warranty will not cover, and no re-imbursement will be
made for such adaptation or any damage which may result.
5.
This warranty covers none of the following:
A.
Periodic check ups, maintenance and repair or replacement of parts due to normal wear
and tear (such as upholsteries, hoses or reduced capacity of accumulators).
B.
Cost relating to transport, removal or installation of the product.
C.
Misuse, including the failure to use this product for its normal purposes or incorrect
installation.
D.
Damage caused by lightning, water, fire, acts of god, war, public disturbances, incorrect
mains voltage or any other cause beyond the control of Hammaplast Medical AB.
E.
Spillage of chemicals or liquid or use of any other hazardous or non instructed
substances, which may affect the product.
F.
Minor defects or deviations from the product specifications, that are immaterial or
negligible as regards to the value or the functioning of the product.
1.5
Copyrights
The manual is an exclusive part of the equipment and may not be provided to or used by any
third party. Pictures, text, specifications and other illustrations are protected by copyright and
may not be copied without approval by Hammarplast Medical AB.
1.6
Customer service
For technical questions, contact Hammarplast Medical customer service. Contact information is
found under chapter 1.3
1.7
CE labeling
The equipment is manufactured in accordance to EU´s directives regarding current medical
equipment 93/42/EEC.
CE labeling is located on the equipment's rear side.
Warning: This instrument, as all medical electric equipment in general, needs special
precautions regarding EMC and needs to be installed and put into service according to
information in this document.
Warning: This instrument, as all portable medical electric equipment in general, can
affect other medical electrical equipment. Refer to Appendix EMC for further guidance
regarding EMC.
Содержание Tourniquet 800-20
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