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14. CONFORMITY
14.1 TESTING & COMPLIANCE
The M9 Transfer stretcher satisfies the requirements of directive 2017/745, 93/42/EEC and UK MDR 2002
for medical devices - Class 1 medical device products.
The M9 Transfer stretcher has been developed to comply with requirements of:
•
IEC60601-1:2005
•
IEC60601-2-52:2009
14.2 IP STANDARDS
•
BS EN 60529:1992.
Specification of degrees of protection provided by enclosures.
IPX4 4 - Protected against water sprayed from all directions, limited ingress permitted.
14.3 RECYCLING
Howard Wright Limited cares for the environment. Our manufacturing facility, based in an ecologically diverse
area, means we are committed to a healthy environment. Please follow the recycling guidelines within your
country.
All packaging, including cardboard and timber can be recycled.
This stretcher is manufactured from steel, aluminium, ABS and nylon plastics, all of which can be recycled.
All electronic equipment should be returned to an approved electrical waste recycling treatment plant.
Batteries are of a sealed lead acid type and must be returned to a specialist battery disposal company.
Please follow the WEEE (2012/19/EU) directive if within the European Community or environmental legislation
in the country of use. Please visit the Environment section of the Howard Wright Limited web site for further
information.
The stretcher complies with the RoHS2 (2011/65/EU) directive.
Please see the Howard Wright Limited website for WEEE and Waste Battery information.
See the M9 Transfer Technical Service Manual for details on disassembly of medical stretchers.
14.4 EXPECTED SERVICE LIFE
The expected service life of the M9 Transfer stretcher is 7 years from the date of manufacture.
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M9 Transfer Instructions For Use (M999-190, Version 1, 2022-04)
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