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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:

l

  Reorient or relocate the receiving antenna.

l

  Increase the separation between the equipment.

l

  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:

l

  Have the interfering equipment repaired or replaced.

l

  Reorient or relocate the interfering equipment.

l

  Increase the separation between the equipment and the possible source of the interference.

l

  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 PC’s 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. From 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 QUATTRO

®

 conforms to 

this IEC60601-1-2 standard for immunity and emission. Nevertheless, special precautions need to be 

observed:

The QUATTRO

®

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

The QUATTRO

®

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

The user of the QUATTRO

®

 should assure that it is used in such environment.

In general, although the QUATTRO

®

 complies too the EMC standards, it can be affected by portable 

and mobile RF communications equipment (such as mobile telephones).

The QUATTRO

®

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

stacked use is necessary, the QUATTRO

®

 should be observed to verify normal operation.

18

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

Emissions Test

Compliance

Electromagnetic environment - guidance

RF emissions CISPR 11

Class B

The QUATTRO

®

 systems are suitable for use in all establishments, 

including domestic establishments and those directly connected to 

the public low-voltage pump supply network that supplies buildings 

used for domestic purposes.

Harmonics emissions 61000-3-2

Class A

Voltage fluctuations / flicker emissions 61000-3-3

Complies

Содержание QUATTROOVERLAY

Страница 1: ...r Pressure Area Care Mattresses and Cushions QUATTRO ACUTE Systems QUATTRO PLUS Systems QUATTRO OVERLAY Systems PULSAIR CHOICE Systems POLYFLOAT SUPREMA POLYFLOAT DORMIRA B A S E Seating Systems reducing avoidable harms ...

Страница 2: ... the user to the possibility of a problem with the system associated with its use or misuse Operating Instructions IP Ingress Protection 2 Protection against fingers or other object not greater than 80mm in length and 12mm in diameter 1 Protection from vertically dripping water IP21 1 Caution Refer to instructions of use booklet Medical Devices Directive 93 42 EEC North America ETL listed Class II...

Страница 3: ...in a cot size version for paediatric use l QUATTRO PLUS mattress replacement system for patients at high risk of pressure ulcers l QUATTRO OVERLAY mattress overlay system for patients at high risk of pressure ulcers l PULSAIR CHOICE mattress replacement for patients at high risk of pressure ulcers l PULSAIR CHOICE mattress overlay for patients at medium risk of pressure ulcers l PULSAIR CHOICE cus...

Страница 4: ...ising or lowering of bed or bed rails or any other moving object l The power unit must only be used with a suitable approved cord and plug set as supplied by Talley l The system is not used in the presence of flammable anesthetics l Suitable for continuous use l Not suitable for sterilisation l Do not position the power unit to make it difficult to disconnect the power supply plug or mattress l Do...

Страница 5: ...r injury l In order for alternating air pressure mattress cushion range to operate effectively please avoid placing objects on the surface that may obstruct the movement of air between the cells For the same reason please discourage people from sitting on the edge or on the end of the mattress whilst it is in use l Do not use abrasive cleaners phenol disinfectants solvents or alcohol based cleanse...

Страница 6: ...ed mattress and causing possible injury to the patient A strap extension kit is available for use with divan beds part number 97 50 10 153 4 Suspend the power unit from the foot board of the bed having first adjusted the hanger brackets as instructed at the rear of the unit Alternatively the power unit may be placed on the floor 5 Attach the air supply hose to the power unit by aligning the black ...

Страница 7: ... screen Press and hold the MUTE UNLOCK button until power unit beeps if further button operation is needed i e change of therapy mode or comfort setting 12 Place the carry bag and user manual in a safe place for future use INSTALLING CUSHIONS The QUATTRO PLUS QUATTRO OVERLAY AND PULSAIR CHOICE power units can all be used to operate their respective alternating air pressure cushions Place the cushi...

Страница 8: ...D The mattress and cushion will operate simultaneously allowing the simple transfer of the patient between the bed and chair NB When the patient is in bed return the comfort setting to the mattress settings of SOFT MEDIUM or FIRM It should be noted that the use of an alternating air pressure cushion will increase the patient s seated height by approximately 5cm and care should be taken to ensure t...

Страница 9: ...g The power unit will lock again 2 minutes after the last button operation NB After power failure switching the power off pressing MUTE cancels the system s previous settings When power returns the default setting of ACTIVE mode MEDIUM comfort setting is invoked Note that previous settings are automatically cancelled if the duration between switch off and switch on is greater than 12 seconds If po...

Страница 10: ...main inflated so supporting the patient All alternating air pressure mattresses can be used on profiling bed frames slatted frames in filled frames and divans Back rests or pillows for support should be placed beneath the mattress to allow uninterrupted body contact with the mattress surface Place the bottom sheet loosely on the mattress to allow the mattress surface greater contact with the patie...

Страница 11: ...rinsed with clean water to remove any residues This will help prevent any possible long term compatibility issues associated with disinfectant residues l Alternatively disinfection may be achieved by laundering at temperatures not exceeding 650 C for 10 minutes or 730 C for 3 minutes which may include a chlorine rinse l Do not use abrasive cleaners phenol disinfectants solvents or alcohol based cl...

Страница 12: ...niversally used on all hard and soft surfaces without any detrimental effect TECcare CONTROL is CE marked for cleaning medical equipment SERVICING Once the initial guarantee period expires Talley recommend that all power units should be serviced annually or as indicated by the hours to service display The unit contains no user serviceable parts and should only be serviced by either Talley or an au...

Страница 13: ...een All systems have a fault log that records the last 5 faults via the DATA display mode If problems reoccur contact Talley AC FAIL fault indicates a mains power failure a sounder will be heard if power is interrupted e g power unit switched off power cut disconnection of mains lead Press MUTE or re connect to power supply ROTOR SYSTEM fault indicates the automatic sequential cycle has stopped or...

Страница 14: ...t by pressing MUTE button EMI FAULT Caused by external RF fields Fault will clear when interference ceases Check air cells and tubing are intact FAULT Reset power unit by pressing MUTE button MATTRESS FLAT no sounder Check that mains power is connected indicated by illuminated LCD display and allow at least 20 minutes for mattress to inflate UNCALIBRATED The system will continue to operate but con...

Страница 15: ... gap of 2 5cm either side of the mattress should not be exceeded when side rails are deployed CUSHIONS Place the POLYFLOAT cushion onto a chair ensuring cushion is placed the correct way up N B It should be noted that the use of a foam cushion will increase the patient s seated height by approximately 5cm and care should be taken to ensure the patient s comfort and security regarding height of foo...

Страница 16: ...is will help prevent any possible long term compatibility issues associated with disinfectant residues l Alternatively disinfection may be achieved by laundering at temperatures not exceeding 650 C for 10 minutes or 730 C for 3 minutes which may include a chlorine rinse l Do not use abrasive cleaners phenol disinfectants solvents or alcohol based cleansers e g Dettol Phenicol Hibiscrub Clearsol St...

Страница 17: ...e Time QUATTRO ACUTE variable continuous QUATTRO PLUS 16 minutes continuous QUATTRO OVERLAY 16 minutes continuous PULSAIR CHOICE 16 minutes mattress replacement 8 minutes mattress overlay cushion continuous ALTERNATING AIR PRESSURE MATTRESSES Medical Device Classification Class IIa Construction BASE QUATTRO ACUTE QUATTRO PLUS QUATTRO OVERLAY Woven nylon 940 DTEX PU coated both sides PULSAIR CHOICE...

Страница 18: ...430mm x 430mm x 70mm UK standard size B A S E RECLINER MAT cushion 1080mm x 430mm x 70mm PULSAIR CHOICE cushion 430mm x 430mm x 40mm Weight B A S E SEQUENTIAL cushion 1 9kg n B A S E RECLINER MAT cushion 3 9kg n PULSAIR CHOICE cushion 1 3kg STATIC FOAM MATTRESSES CUSHIONS Medical Device Classification Class I Construction POLYFLOAT SUPREMA mattress base frame CMHR foam 38 40kg m3 175 215 blue inse...

Страница 19: ...fering equipment repaired or replaced l Reorient or relocate the interfering equipment l Increase the separation between the equipment and the possible source of the interference l 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 ...

Страница 20: ... separation distance in meters 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 Note1 At 80 MHz and 800 MHz the higher frequency range applies Note2 These guidelines may not apply in all situations Elec...

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