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Safety Information - NEUROTECH Recovery-Back Manual Del Usuario

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Safety Information

Validity
The information and technical data contained in this document relates to the Neurotech Recovery - Back conductive garment
system with this manual. The information and technical data disclosed in this document are proprietary to Neurotech and may
be used and disseminated only for the purposes and to the extent specifically authorized in writing by the company.
Disclaimers
All equipment manufactured and sold by Neurotech, a Division of Bio-Medical Research Ltd., are rigorously checked and tested
prior to shipment. However, the use of this equipment is outside of the control of the company. Neurotech only accepts
responsibility for the safety, reliability and performance of the equipment when it is operated in accordance with the instructions
herein and within the given specifications. Therefore, the user must bear full responsibility for any actions arising out of the use
or misuse of this equipment. Any modifications, repairs or servicing must be undertaken by authorized Neurotech personnel.
Restrictions
The sale and/or operation of this equipment is subject to law in the various states/countries. Compliance with this legislation
rests with the importer, dealer, or user of the equipment as appropriate.
Indications For Use - Neurotech Recovery - Back
The Neurotech Recovery – Back conductive garment for the back and associated accessories are indicated for use with
Neurotech Stimulators to facilitate the frequent and correct positioning and repositioning of large, multiple, and/or difficult to
reach stimulation sites associated with the low back.
The Neurotech Recovery – Back conductive garment for the abdomen and associated accessories are indicated for use with
Neurotech Stimulators to facilitate the frequent and correct positioning and repositioning of large, multiple, and/or difficult to
reach stimulation sites associated with the abdominal area.
Prescription Required:
Caution: In the United States of America federal law restricts the device to sale or use by, or on the order of, a physician or other
practitioner licensed by the laws of the state in which he/she practices.
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