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19
ENGLISH
0197
IIa Class Medical Device
According to directive 93/42/EEC and further modifications
1. CODES
LTM560
Modulable therapy pump with LCD display
LTM563-S
Sleeve S/M
LTM563-L
Sleeve L/XL
LTM566-S
Boot S/M
LTM566-L
Boot L/XL
LTM568
Extension
LTM569
Abdominal band
2. INTRODUCTION
Thank you for purchasing a compression therapy Advance LEM by Moretti S.p A. designed and
built to meet all your needs for a correct, safe and practical use. This user’s manual provides
some suggestions as how to correctly use the product you have chosen and gives some valuable
advice for your safety. Please read through the manual carefully before using the product. Should
you have any queries, please contact your retailer for advice and assistance. In case of doubts,
please contact the dealer, who will help and advise you properly.
3. INTENDED USE
Advance compression therapy is a device intended for patients who need a lymphatic drainage in
the limbs, i.e. it increases the lymph drainage from congested areas facilitating the body’s natural
skill to eliminate toxins.
WARNING!
The pressure therapy is a medical device, in the presence of any health problem
use the device only after consulting your doctor.
• Don’t use the device for a purpose not indicated in the present manual.
• Moretti S.p.A. declines all responsibilities for any consequences resulting from
improper use of the device or from an unauthorized alteration of the device.
• The manufacturer reserves the right to make changes to the device and to this
manual without notice in order to improve its features.
4. EC DECLARATION OF CONFORMITY
Moretti S.p.A. Declares under his sole responsibility that the product marketed by the same Moretti
S.p.A. Is in accordance to the relevant provisions of Directive 93/42/EEC on medical devices and
subsequent amendments and are produced by xiamen senyang co ltd according to the standards set
out in the below standards:
Standards and directives
The pressure therapy Advance has been tested and approved according to the following
guidelines and standards:
Safety standard EN 60601-1 Medical electrical equipment part 1: General requirements for safety
EMC standard EN 60601-1-2 - Medical electrical equipment part 1: General requirements
for safety- Collateral standard: Electromagnetic compatibility - Requirements and tests
EN 60601-1-11 Medical electrical equipment part 1: General requirements for basic safety and
essential performance