BMB MEDICAL
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TIM
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VERSION 1
57
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Do not use the MD on a floor with a slope of more than 10%.
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To avoid the risk of patient or user injury of IV pole damage when moving the chair,
ensure that the IV pole is firmly secured.
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To avoid damaging the equipment during transport, ensure that the IV pole passes safely
through all door frames and under all light fittings.
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Never use the chair in the presence of an anesthesia mixture flammable with air, with
oxygen, or with nitrous oxide as this could cause a fire and/or explosion.
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To prevent failure, electromedical equipment requires special
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Do not manually raise the legrest.
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Work on electrical parts should only be performed by qualified and authorized staff.
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Used to accommodate a person of small stature (less than 1.30 m tall), or under the age
of 12 years.
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Do not alter the chair. Any changes made to the system could lead to unpredictable
operation that could in turn jeopardize the safety of the user or patient. This would also
void the chair’s warranty.
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To avoid material damage or injury, do not use the IV pole to pull or push the product.
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To avoid damaging the equipment, the maximum permissible load of the IV pole is 6 kg.
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Use by a person who has not first familiarized themselves with this user manual.
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Use by any non-caregiver who has not received the authorization and explanations from
a qualified individual.
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Use of the chair with a load that exceeds the safe working load (see technical
characteristics).
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Use outside of the establishment, or on unprepared ground.
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Washing with large amounts of water, with a high-pressure jet or with steam and
passage through a wash tunnel.
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Connection, by any means, of an electric device to the chair.
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Any use that does not fall within the operating context of a hospital chair.
All manipulations relating to the aforementioned precautions for use are described in
paragraph II - Instructions for Use HERE.
4.1.2
CONTRAINDICATIONS
There are no other contraindications for this device
4.1.3
PRECAUTION ASSOCIATED WITH EQUIPMENT CARE AND MAINTENANCE
The device must not be altered in any way without the manufacturer’s prior consent: the alteration
could lead to unpredictable operation, potentially injuring the patient and caregivers.
Torn upholstery no longer presents an effective antibacterial barrier and must hence be replaced
as soon as possible.
The device must be regularly inspected, at least twice per year.