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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

8.5 EMI/EMC Statement and Manufacturer’s Declaration

This equipment has been tested and found to comply with the limits of EN 60601-1-2.

These limits are designed to provide reasonable protection against harmful interference in both a medical and 
residential environment. This equipment generates, uses and can radiate radio frequency energy and, if not used in 
accordance with manufacturer’s instructions, may cause harmful interference to radio communications. However, 
there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful 
interference to radio or television reception or other equipment, which can be determined by turning the equipment off 
and on, the user is encouraged to try to correct the interference by one of the following measures:
•  Reorient or relocate the receiving antenna.
•  Increase the separation between the equipment.
•  Connect the equipment to an outlet on a circuit different from that to which the receiver or equipment was 

connected.

The equipment having been tested to operate within the limits of electromagnetic compatibility. (Immunity to 
interference from nearby sources radiating radio frequency energy). Sources exceeding these limits may give rise 
to operation faults. Where possible the system will sense the interference and if it is of short duration transparently 
take countermeasures whilst operating near normally, or failing this will issue a warning and take measures for the 
continued safely of the user. Further increased levels of energy may cause the system to stop operating, continuously 
generate random faults or continuous 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 correct the interference by one of the following 
measures:
•  Have the interfering equipment repaired or replaced.
•  Reorient or relocate the interfering equipment.
•  Increase the separation between the equipment and the possible source of the interference.
•  Connect the equipment to an outlet on a circuit different from that to which the interfering equipment was 

connected.

Information regarding Electro Magnetic Compatibility (EMC) according to IEC60601-1-2

With the increased number of electronic devices such as PCs and mobile telephones, medical devices in use may be 
susceptible to electromagnetic interference from other devices. The EMC (Electro Magnetic Compatibility) standard 
IEC60601-1-2 defines the levels of immunity to these electromagnetic interferences. On the other hand, medical 
devices must not interfere with other devices. IEC60601-1-2 also defines the maximum levels of emissions for these 
medical devices. The 

VENTURI

 conforms to this IEC60601-1-2 standard for immunity and emission. Nevertheless, 

special precautions need to be observed:
•  The 

VENTURI

 needs to be installed and put into service according to the EMC information below.

•  The 

VENTURI

 is intended for use in the electromagnetic environment specified in the tables below. The user of 

the 

VENTURI

 should assure that it is used in such environment.

•  In general, although the 

VENTURI

 complies to the EMC standards, it can be affected by portable and mobile RF 

communications equipment (such as mobile telephones).

•  The 

VENTURI

 should not be used adjacent to or stacked with other equipment. In case adjacent or stacked use 

is necessary, the 

VENTURI

 should be observed to verify normal operation.

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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