Foreword; Intended User/Operator; Product Liability; Installation - Enraf Nonius Manumed Tilt Manual De Uso

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  • MX

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  • MEXICANO, página 45

1 Foreword

1.1

Intended User/Operator

We are pleased that you have purchased a Manumed special tilt table. The Manumed special tilt table is
specially designed to allow continuous tilt settings from horizontal through the vertical position. The
variable height option allows easy patient transfer from either a wheelchair or bed. The Manumed special
tilt table is especially suitable for the management of circulatary problems associated with long term
immobilization and relief to patients with decubitus ulcers. It gives standing support during
ergotherapeutic exercise and provides controlled and progressive load applications to accustom patients
to artificial limbs. Post-operative conditions involving the lower extremities, atonic paresis and badly
healing fractures also benefit from using the Manumed special tilt table.
During development and production of this table, great care and attention has been put into the reliability,
safety, ease of use and durability. It is important to read the following instructions carefully before using
the Manumed special tilt table.
This operating instructions deals with:
Manumed Special Tilt 1-section (typ 722 and 723)
Manumed Special Tilt 2-section (typ 724 and 725)
1.2

Product Liability

A law on Product Liability has become effective in many countries. This Product Liability law implies,
amongst other things, that once a period of 10 years has elapsed after a product has been brought into
circulation, the manufacturer can no longer be held responsible for possible shortcomings of the product.
To the maximum extent permitted by applicable law, in no event will Enraf-Nonius or its suppliers or
resellers be liable for any indirect, special, incidental or consequential damages arising from the use of or
inability to use the product, including, without limitation, damages for loss of goodwill, work and
productivity, computer failure or malfunction, or any and all other commercial damages or losses, even if
advised of the possibility thereof, and regardless of the legal or equitable theory (contract, tort or
otherwise) upon which the claim is based. In any case, Enraf-Nonius's entire liability under any provision
of this agreement shall not exceed in the aggregate the sum of the fees paid for this product and fees for
support of the product received by Enraf-Nonius under a separate support agreement (if any), with the
exception of death or personal injury caused by the negligence of Enraf-Nonius to the extent applicable
law prohibits the limitation of damages in such cases.
The opposing party (product's user or its representative) shall disclaim Enraf-Nonius from all claims
arising from third parties, whatever nature or whatever relationship to the opposing party.

2 Installation

1.
Take the Manumed and any extra parts out of the cardboard packaging and check everything for
possible transport damage.
2.
Read this manual carefully before using the equipment.
3.
Mains supply connections must comply with the national requirements regarding medical rooms.
4.
Prior to connection of this apparatus to the mains supply, check that the voltage and frequency
stated on the type plate correspond with the available mains supply.
5.
Avoid exposure to direct sunlight, UV radiation, rain, excessive dust, moisture, mechanical
vibrations and shocks.

3 General instructions

1.
This equipment complies with all requirements of the Council Directive 93/42/EEC of the
European Community, concerning medical devices. The intended use (and the prescribed
application) of this device is stricktly reserved to medical professionals. The accessibility of this
device and the precautions for prevention of unsupervised or illicit use has to be guaranteed by
the institute or medical professional to whom the device is delivered or to whom permission of use
is granted. Enraf-Nonius B.V. cannot be held responsible for any consequences of unlawful use
of this device.
1

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