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Emissions Test

IEC 60601-

1-1

Test Level

Compliance

Level

Electromagnetic 

Environment Guidance

Electrostatic 

discharge

(ESD)

IEC 61000-4-2

± 6 kV

contact

± 8 kV air

± 6 kV

contact

± 8 kV air

Floors should be wood,

concrete, or ceramic tile. 

If 

fl

oors are covered with 

synthetic material, the 

relative humidity should be 

at least 30 %

Electrical fast

transient/burst

IEC 61000-4-4

Not

Applicable

Not Applicable

Not Applicable

Surge

IEC 61000-4-5

Not

Applicable

Not Applicable

Voltage dips, 

short

interruptions 

and

voltage 

variations

on power supply

input lines

IEC 61000-4-11

Not Applicable

Not Applicable

Power frequency

(50/60 Hz)

magnetic 

fi

eld

IEC 61000-4-8

3 A/m 3

3 A/m 3

Power frequency magnetic 

fi

elds should be at levels

characteristic of a typical 

location in a typical

domestic, commercial

or hospital environment.

Emissions Test

Compliance

Electromagnetic Environment Guidance

RF emissions

CISPR 11

Group 1

The device does not use RF for its function.

Therefore, its RF emissions are very low and are 

not likely to cause any interference in nearby 

electronic equipment.

RF emissions

CISPR 11

Class B

The device is suitable for use in all 

establishments, including domestic 

establishments and those directly connected to 

the low voltage power

supply network that supplies buildings used for 

domestic purposes.

Harmonic 

emissions

IEC 61000-3-2

Not applicable

Voltage 

fl

uctuations/

fl

icker emissions

IEC 61000-3-3

Not applicable

Guidance and Manufacturer’s Declaration 

Electromagnetic Emissions

IEC 60601-1-2 for the Tendonworks and Accel-Heal® Devices

 

The device is suitable for use in the speci

fi

ed electromagnetic 

environment. The customer and / or the user of the device should assure 

that it is used in an electromagnetic environment as described below:

Guidance and Manufacturer’s Declaration 

Electromagnetic Immdevicey

IEC 60601-1-2 Tendonworks and Accel-Heal® Devices

Immunity

test

IEC

60601

test 

level

Compliance

level

Electromagnetic

environment – guidance

Conducted

RF

IEC 61000-

4-6

3Vrms

150kHz 

to

80 MHz

3Vrms

Portable and mobile RF communications 

equipment should be used no closer to any 

part of the device, including cables, than 

the recommended separation distance 

calculated from the equation applicable to 

the frequency of the transmitter. 

Recommended separation distance:

 

 

 

where P is the maximum output power rating 

of the transmitter in watts (W) according to 

the transmitter manufacturer and d is the 

recommended separation distance in metres 

(m). Field strengths from 

fi

xed RF transmitters, 

as determined by an electromagnetic site 

survey,a should be less than the compliance 

level in each frequency range. Interference 

may occur in the vicinity of equipment 

marked with the following symbol:

Radiated RF

IEC 61000-

4-3

3 V/m

80 MHz 

to

2,5 GHz

3 V/m

80 MHz

to 

2.2 GHzw

Guidance and Manufacturer’s Declaration 

Electromagnetic Immunity for Tendonworks and Accel-Heal® Devices

 

The device is intended for use in the electromagnetic environment 

speci

fi

ed below. The customer and / or the user of the device should 

assure that it is used in such an environment.

Immunity

test

IEC

60601

test 

level

Compliance

level

Electromagnetic

environment – guidance

test

If abnormal performance is observed 

such as the device turning o

ff

, additional 

separation distance or screening may 

be necessary.

NOTE 1:

At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2:

These guidelines may not apply in all situations. Electromagnetic propagation is 

a

ff

ected by absorption and re

fl

ection from structures, objects and people.

Field strengths from 

fi

xed transmitters, such as base stations for radio (cellular/cordless) 

telephones and land mobile radios, amateur radio, AM and FM radio broadcast 

and TV broadcast cannot be predicted theoretically with accuracy. To assess the 

electromagnetic environment due to 

fi

xed RF transmitters, an electromagnetic site 

survey should be considered. If the measured 

fi

eld strength in the location in which 

the device is used exceeds the applicable RF compliance level above, the device should 

be observed to verify normal operation. If abnormal performance is observed such as 

the device turning o

ff

, additional measures may be necessary, such as reorienting or 

relocating the device.
Over the frequency range 150kHz to 80MHz, 

fi

eld strength should be less than 3V/m.

Rated maximum 

output power of 

transmitter

Separation distance according to frequency of transmitter

150 kHz to 80 MHz

Not Applicable

80 MHz to 

800 MHz

800 MHz to 

1.4 GHz

0.01

0.12

0.12

0.23

0.1

0.37

0.37

0.74

1

1.2

1.2

2.3

10

3.7

3.7

7.4

100

12

12

23

For transmitters rated at a maximum output power not listed above, the

recommended separation distance d in metres (m) can be estimated using the

equation applicable to the frequency of the transmitter, where P is the maximum

output power rating of the transmitter in watts (W) according to the transmitter

manufacturer.

NOTE 1

: At 80 MHz and 800 MHz the separation distance for the higher frequency 

range applies.

NOTE 2:

 These guidelines may not apply in all situations. Electromagnetic propagation 

is a

ff

ected by absorption and re

fl

ection from structures, objects and people.

Symbol Used

Meaning

Caution

Keep Dry

Keep Out of Direct Sunlight

Temperature Limitation

Single Use Only - Do 

NOT

 Reuse

WEEE Directive 2002/96/EC Compliant

106kPa

50kPa

Atmospheric Pressure Limitation

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95%

Humidity Limitation

Type BF protection against electric 

shock

Recommended Separation Distances 

Between portable and mobile RF communications equipment 

and the Tendonworks and Accel-Heal® devices

 

The device is intended for use in an electromagnetic environment in 

which radiated RF disturbances are controlled. The customer or the 

user of the device can help prevent electromagnetic interference 

by maintaining a minimum distance between portable and mobile 

RF communications equipment (transmitters) and the device as 

recommended below, according to the maximum output power of the 

communications equipment.

Glossary of Symbols Used

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Manufactured by:
Synapse Electroceutical Ltd. UK
1 Churchill Court, Hortons Way, 
Westerham, Kent TN16 1BT,
England, UK.
Tel:  +44 (0)1959 569 433
Fax: +44 (0)1959 565 281
Email: [email protected]
www.accelheal.com

Revision No: 8 Date of Issue:28th  September 2015

Pregnancy

 

There is no evidence to suggest that the Synapse Elec-

troceutical device would be detrimental to a healthy 

pregnancy. However, based upon precautionary meas-

ures, we suggest that you consult your physician before 

using the device.

Serious Disease 

If you su

ff

er from a serious disease or condition such as 

cancer we suggest you consult your physician before 

using the device.

Epilepsy

 

If you su

ff

er from epilepsy we advise that you do not 

use the device near the head.

Varicose Veins / Main Arteries 

Do not place electrode pads directly over broken capil-

laries or varicose veins. We also advise that you do not 

place electrode pads directly over main arteries such as 

the carotid arteries in the neck.

Water

 

As with all electrical devices do not use the Synapse 

Electroceutical device when bathing or if the device 

becomes wet.

Children

 

The device and the accessories should be kept out of 

the reach of children.

ECGs and other electrical devices

 

When the Synapse Electroceutical treatments are in 

progress they may interfere with ECG and EEG monitors 

and alarms.

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Interference

 

Please be aware there may be interference from other 

electronic devices that a

ff

ect the performance of the 

Synapse Electroceutical device and it may a

ff

ect other 

electronic devices. If there are problems please switch o

ff

 

the o

ff

ending device or increase their separation distance.

Electrode Pads 

We advise that you use electrode pads which comply with 

MDD* safety standards (*Medical Device Directive). These 

are available directly from Synapse Electroceutical Ltd.

  No unauthorised extension leads, cables or attachments 

should be used with the device.

Environmental Conditions for Transport, Storage and

Operation

 

Please ensure storage transportation and operation is 

within 0°C ~ 45°C and less than 95% humidity. 

Please ensure device is stored and transported between 

50 -106 kPa 

Please ensure device is operated between 70 - 106 kPa 

Cleaning

 

For optimum performance always ensure that the Synapse 

Electroceutical device is kept in a clean condition. We sug-

gest cleaning with a mildly damp cloth; ensure that water 

does not penetrate the device.

  For a comprehensive document covering hazards, 

contra-indications and warranty please visit:

  www.accelheal.com/support.html

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50kPa

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