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D H G - H E A LT H C A R E . C O M

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U S E R   M A N U A L

Guidance and Manufacturer’s Declaration: Electromagnetic Immunity (IEC 60601-1-2)

Immunity Test

IEC 60601 Test 

Level

Compliance Level

Electromagnetic

Environment - Guidance

Conducted RF
IEC 61000-4-6

Radiated RF
IEC 61000-4-3

3 V rms
150 kHz ~ 80 MHz

6 V rms
150 kHz to 80 MHz
in ISM and amateur 
radio bands between 
0,15 MHz and 80 
MHz

10 V/m
80 MHz ~ 2.7 GHz

3 V rms

6 V rms

10 V/m

Field strengths from fixed RF 
transmitters as determined by 
an electromagnetic site
survey,

a

 should be less than 

the compliance level in each 
frequency range.

b

Interference may occur in the 
vicinity of equipment marked 
with the following symbol:

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 affected by absorption and 
reflection from structures, objects, and people.

a

 Field strengths from fixed transmitters, such as base stations for radio (cellular/ cordless) telephones and land 

mobile radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To 
assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be 
considered. If the measured field strength in the location in which the VENTURI is used exceeds the applicable RF 
compliance level above, the VENTURI should be observed to verify normal operation. If abnormal performance is 
observed, additional measures may be necessary, such as reorienting or relocating the VENTURI.

b

 Over the frequency range 150 kHz to 80MHz, field strengths should be less than 3 V/m.

Declaration – Electromagnetic Immunity

Every care has been taken to ensure that the information contained in this manual was correct at the time of going 
to press. However, Direct Healthcare Group reserves the right to modify the specification of any product without prior 
notice in line with a policy of continual product development. Information is available in alternative formats on request.

Our standard terms and conditions apply.

Содержание TG600/14

Страница 1: ...DHG HEALTHC AR E C O M DHG HE ALTHCAR E C O M VENTURI MINO User Manual...

Страница 2: ...VENTURI MINO DHG HEALTHCARE COM...

Страница 3: ...tions and Information 4 4 How to Apply NPWT 5 Getting Started 5 Operating the Vacuum Power Unit 5 5 Operation Guidelines 6 User Information 6 Operation Controls 7 Battery Information 7 6 Care and Main...

Страница 4: ...n Warning Refer to instruction manual booklet Medical Devices Directive 93 42 EEC Medical Device Regulation 2017 745 North America ETL listed Class II Equipment Double Insulated Do not dispose of with...

Страница 5: ...gery Wounds which may benefit from the application of NPWT include pressure ulcers dehisced surgical wounds diabetic neuropathic foot ulcers venous leg ulcers post op surgical wounds including flaps a...

Страница 6: ...near to material which is flammable or can be damaged by heat The supplied power adapters plug directly into the power source partly mitigating this issue The VENTURI MINO TG600 14 vacuum power unit...

Страница 7: ...o the VENTURI MINO power unit by lining up the two parts pushing together and twisting to lock Fig 1 Remove the bung from the connector port this can be retained to cap the used canister prior to disp...

Страница 8: ...ubing as above this can be reconnected to new canister and unclamped if wound dressing is not being changed Rotate canister to unlock and remove from power unit Dispose of used canister according to l...

Страница 9: ...begin operation at the default pressure of 80mmHg The selected vacuum level is shown on the display screen 5 3 Battery Information A fully charged battery should operate the power unit continuously fo...

Страница 10: ...ocial care facilities TECcare CONTROL products provide class leading broad spectrum high level disinfection with an exceptional safety profile Being pH neutral TECcare CONTROL can be universally used...

Страница 11: ...heck that low flow is not caused by pinched or bent tubing If exudate is pooling in the wound bed the dressing should be changed This alert will self cancel after 5 minutes and will re occur if the co...

Страница 12: ...above mains adapter is considered part of the ME equipment The VENTURI MINO power unit must only be used with the specific external power adapter as supplied by Direct Healthcare Group EXPECTED SERVIC...

Страница 13: ...ntinuous resets Try to ascertain the source of the interference by turning nearby or suspect equipment off and see if the interference effects stop In any such event the user is encouraged to try to c...

Страница 14: ...UT 0 5 cycle At 0 45 90 135 180 225 270 and 315 Mains supply quality for the mains adapter should be that of a typical commercial and or hospital environment In the event of a mains interruption the V...

Страница 15: ...rs such as base stations for radio cellular cordless telephones and land mobile radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electroma...

Страница 16: ...et Swatar BKR 4013 Malta Direct Healthcare Group Ltd Withey Court Western Industrial Estate Caerphilly United Kingdom CF83 1BF T 44 0 800 043 0881 F 44 0 845 459 9832 E info directhealthcaregroup com...

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