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The following symbols may appear in this manual or on the machine. Some of  
the symbols represent standards and compliances associated with the machine  
and its use.

Caution: Consult accompanying documents

CE Mark: conforms to essential requirements of the Medical Device Directive  
93/42/EEC.

CE Mark: conforms to essential requirements of the R&TTE Directive 1999/5/EC

Date ofmanufacture.

Manufacturer

Type B applied part

DISPOSAL: Do not dispose this product as unsorted municipal waste. Collection  
of such waste separately for special treatment is necessary.

CB Certification Scheme

C-TICK Certification from the Australian Communications Authority

GOST - Standard of Russia

Compliant with RoHS Directive 2002/95/EC

CQC Safety and EMC Product Certification Mark

Compliance with DENAN law Japan

Symbol Descriptions

Follow instructions foruse

14 of 22

15 of 22

Safety Classification

1. Class I equipment;
2. Type B applied part;
3. IPX0;
4. Not category AP / APG equipment;

5. For 60601-1 2nd edition, Mode of operation: Short Time Operation : Max. of 4  

minutes / This is for North America and Canada

6. For 60601-1 3rd edition, Mode of operation: Non-continuous Operation : 9 mins

on/ 3 hours off / This is for Europe

Environmental Requirements

OPERATINGCONDITIONS
Temperature: 10ºC to40ºC  
Humidity: 10% to 95% RH
Pressure altitude: Normal atmospheric

conditions/ 860-1060hPa

STORAGE AND SHIPPINGCONDITIONS
Temperature: 10ºC to40ºC  
Humidity: 10% to 95% RH
Pressure altitude: Normal atmospheric

conditions/ 860-1060hPa

WARNING

The device is not suitable for use in the presence of flammable anesthetic mixtures  
with air or with oxygen or nitrous oxide.

The device requires no calibration.
The device is not repairable and contains no user serviceable parts.

The user must check that the equipment functions safely and see that it is in  

proper working condition before being used.

The manufacturer does not require such preventive inspections by other persons.

The plug is used to disconnect from the main supply. Do not position the machine  
so that it is difficult to disconnect the main plug.

Warning: To avoid the risk of electric shock, this equipment must only be  

connected to a supply main with protective earth grounding.

Users

The machine is intended for use by a diverse patient population including:

Adult men and women who are medically cleared and able to undertake
physical exercises such as weight bearing and ground reaction force type
exercise programs. In general this applies to healthy adults (16+ years old).

All others users should be cleared by their physician and only use Power Plate  
under medical supervision.

Facilities

The device is intended to be used in all types of facilities including, but not limited  
to:

Domestic

Hotels, Spas, Resorts

Health Clubs

Hospitals, Clinics

Rehabilitation Centers

Active Aging Communities

Содержание pro7

Страница 1: ...pro7 Model...

Страница 2: ...our body Over time the intensity and duration can be in creased in the same manner as other progressive training programs Once the body h as adapted to vibration the training can be changed or intensi...

Страница 3: ...andCardiovascular Claim Power Plate training can be a ben eficial tool intervention to improve and i ncrease circulation and improve the func tion of the cardiovascular system Definit ion The circulat...

Страница 4: ...e is not repairable and contains no user serviceableparts The user must check that the equipment functions safely and see that it is in proper working condition before being used The manufacturer does...

Страница 5: ...s should be used within the normal r ange and angle to maximize training ef fect and prevent damaging the device T he cables should be used between 90 degrees and 25degrees from the horizontal base Te...

Страница 6: ...re thatth eoutletisreceivingelectricalpower If the console display is illuminated but the platform will not vibrate unplug the machine wait at least one minute then check the connection to the machine...

Страница 7: ...meror the user of Pro7should assure that it isused in such an environment NOTE UTis the a c mains voltage prior to application of the test level Immunitytest IEC60601testlevel Compliancelevel Electrom...

Страница 8: ...establishments including domestic establishments and those directly con nected to the public low voltage pow er supply network that supplies buildi ngs used for domestic purposes Both models have bee...

Страница 9: ...rmalatmospheric conditions 860 1060hPa STORAGE AND SHIPPINGCONDITIONS Temperature 10 C to40 C Humidity 10 to 95 RH Pressure altitude Normalatmospheric conditions 860 1060hPa WARNING The device is not...

Страница 10: ...h the instructions supplied This device complies with FCC radiation exposure limits set forth for an uncontrol led environment In order to avoid the possibility of exceeding the FCC radio freq uency e...

Страница 11: ...t directly influence the intensity feltby the user but the duration of the exercis e Intensity level The intensity on the machine can be determined by multiplying frequency and a mplitude The platform...

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