End Of Life Disposal; Warranty And Service - Arjo Pentaflex Bedienungsanleitung

End of Life Disposal

The following advice is recommended:
• Fabric material used on the mattresses
or any other textiles, polymers or plastic
materials etc. should be sorted as
combustible waste.
• Mattresses at the end of life should be
disposed of as waste according to the
national or local requirements which may
be landfill or combustion.
Note: Follow all local regulations and, if
applicable, healthcare facility standard
operating procedures.
Symbols
Recommended wash temperature:
15 min at 60°C
Maximum wash temperature: 15 min
at 95°C
Do not iron
Do not use phenol-based cleaning
solutions
Hospital name
Tumble dry at 60°C
60°C
Maximum drying temperature 80°C
Max 80°
Wipe all surfaces with cleaning solution,
then wipe with a cloth moistened with
water and dry throughly.
Date of first use
UK Symbol explanation
This section is only applicable to United Kingdom (UK) market when UK marking is applied to the Arjo
medical device labelling.
UK Responsible Person & UK Importer:
Arjo (UK) Ltd, ArjoHuntleigh House, Houghton Regis. LU5 5XF
Is the appointed UK Responsible Person as defined in UK Medical Devices Regulations 2002 (SI 2002
No 618, as amended).
For Northern Ireland (NI) CE marking will still apply until further amendment to applicable regulations.
UK marking indicating conformity with UK Medical Devices Regulations
2002 (SI 2002 No 618, as amended)

Warranty and Service

Standard terms and conditions apply to all
sales. A copy is available upon request. These
contain full details of warranty terms and do
not limit the statutory rights of the consumer.
For service, maintenance, and any questions
regarding this, or any other product, please
contact your local distributor.
Operating instructions - Consult
Instructions for use.
Routine disinfection: 1,000 ppm.
Fire retardancy
Safe Working Load (SWL)
250-450 kg / 551-992 lb
CE marking indicating conformity with
European Community harmonised
legislation
Indicates the product is a Medical
Device according to EU Medical Device
Regulation 2017/745
Unique device identifier.
EN
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