TensCare mynd User manual

0

1
Dear Customer,
Thank you for choosing Mynd. TensCare
stands for high-quality, thoroughly tested
products for the applications in the areas
of gentle electrotherapy, muscle toning,
continence management and pain relief
during labour.
Please read these instructions for use
carefully and keep them for later use, be
sure to make them accessible to other
users and observe the information they
contain.
Best regards,
Your TensCare Team

2
CONTENTS
1. INTENDED USE ................................. 5
2. CONTRAINDICATIONS, WARNINGS
& CAUTIONS............................................... 5
3. PROGRAMMES ............................. 12
3.1. PROGRAMME SETTINGS ... 12
3.2. GEL PAD ADVICE.............. 13
4. CONTENT....................................... 14
5. UNIT INFORMATION...................... 14
5.1. CONTROLS......................... 14
5.2. OPERATING INSTRUCTIONS
15
6. SETTING UP AND USING MYND ... 17
6.1. CHARGING THE BATTERY . 17
6.2. PREPARING FOR SESSION 21
6.3. TREATMENT SESSION ......... 23
6.4. AFTER YOUR TREATMENT
SESSION 24
7. CLEANING & STORAGE ............... 24
8. EMC ............................................... 25
9. DISPOSAL OF WASTE ELECTRICAL
AND ELECTRONIC PRODUCTS (WEEE)... 25
10. ACCESSORIES ......................... 26
11. WARRANTY.............................. 27
12. TROUBLESHOOTING................ 30
13. GENERAL SPECIFICATION ...... 31

3
SYMBOLS USED
TYPE BF APPLIED PART: Equipment
providing a degree of protection
against electric shock, with isolated
applied part. Indicates that this
device has
conductive contact
with the end user.
This symb
ol on the unit means
“Refer to instructions for use”.
Temperature Limitation: indicates
the temperature limits to which the
medical device can be safely
exposed.
Lot Number: indicates the
manufacturer’s batch code so that
the batch or lot can be identified.
Humidity Limitation: indicates the
humidity limits to which the medical
device can be safely exposed.
Serial Number: indicates the
manufacturer’s serial number so
that a specific medical device can
be identified.
Do not dispose in household waste.
Catalogue Number: indicates the
manufacturer’s catalogue number
so that the device can be
identified.
Atmospheric Pressure: indicates the
atmospheric limits to which the
medica
l device can be safely
exposed.
Medical Device

4
Manufacturer Symbol
Date of Manufacture: indicates the
date which the medical device
was manufactured. This is included
within the serial number found on
the travel case, either as
“E/Year/Number” (YY/123456) or
“E/Month/Year/Number”
(MM/YY/123456).
CE Mark
This medical device is indicated for
home use.
This medical device is not water
resistant and should be protected
from liquids.
The first number 2: Protected
against access to hazardous parts
with a finger, and the jointed test
finger of 12 mm ø, 80 mm length,
shall have adequate clearance
from hazardous parts, and
protected against solid foreign
objects of 12.5 mm ø and greater.
The second number 2: Protected
against vertically falling water
drops when enclosure is tilted up to
15˚. Vertical
ly falling drops shall
have no harmful effects when the
enclosure is tilted at any angle up
to 15˚ on either side of the vertical.