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The  person  responsible  for  every  day  maintenance  can  substitute  the  spare  parts  indicated  on 
paragraph  6.2  “Spare  Parts”,  only  if  authorized  by  the  manufacturer  or  by  a  centre  authorised  by 
Spencer. 
 
Use only accessories/original spare parts approved by Spencer Italia S.r.l., otherwise we will accept 
no responsibility for the incorrect functioning and/or damage caused by the use of any device which 
has  not  been  repaired,  or  certified  on  expiry  date  by  the  Manufacturer  or  by  one  of  the 
Manufacturer's Authorised Service centres. Warranty will be considered void in compliance with the 
Medical Device Directive 93/42/EEC. 
 

5.2.1

 

Periodic maintenance  

The device must be serviced by the Manufacturer or by an authorised centre every year. 
If above mentioned revision is not carried out the conformity to the Directive 93/42/CE for medical 
devices will no longer be valid therefore, even though the CE mark if present, it is possible that the 
device no longer answers all the requirements as indicated by the Manufacturer at purchase.  
Spencer Italia S.r.l. will take no responsibility the incorrect functioning or any damage caused by a 
device that has not undergone regular revision. 
For any operations that are not carried out directly by the Manufacturer but by an authorised centre, 
we have to underline that a report regarding all operations carried out must be requested. This will 
permit  both  Spencer  Italia  S.r.l.  and  the  end  user  to  keep  a  log  book  regarding  the  operations 
carried out on the device. 

 
5.2.2

 

Special servicing 

Only  the  Manufacturer  or  centres  with  written  authorisation  are  authorised  to  complete 
any special servicing operations. 

For any operations that are not carried out directly by the Manufacturer but by an authorised centre, 
we have to underline that a report regarding all operations carried out must be requested. This will 
permit  both  Spencer  Italia  S.r.l.  and  the  end  user  to  keep  a  log  book  regarding  the  operations 
carried out on the device. 
The  device,  if  used  as indicated in  the  following instruction  manual,  has  an  average  life  span  of  5 
years. The life span can be expanded only following a general revision of the product that must be 
carried out by the Manufacturer or by a centre authorised by the Manufacturer. 
Spencer Italia S.r.l. will accept no responsibility for the incorrect functioning and/or damage caused 
by  the  use  of  any  device  which  has  not  been  repaired,  or  certified  on  expiry  date  by  the 
Manufacturer or by one of the Manufacturer's Authorised Service centres, making void the guarantee 
and the conformity to the Medical Devices Directive 93/42/CEE. 
 

6. ACCESSORES AND SPARE PARTS 

 

6.1

 

Accessories 

There aren’t any accessories for this product. 

 

6.2 

Spare parts 

ST42021A 

Black wheel Ø200 mm 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Содержание 480

Страница 1: ...uality system for the production and the final control of the products certified by the notifying body TÜV SÜD Product Service GmbH INDEX General information page 2 Warnings page 2 Product description page 5 Operating instructions page 7 Maintenance and cleaning page 8 Accessories and spare parts page 10 First edition 20 05 10 Rev 0 20 05 10 ...

Страница 2: ...s indicate the lot number LOT shown on the label applied on the box or on the device 1 5 Demolition When the devices are no more suitable for being used if they haven t been contaminated by any particular agents they can be disposed of as normal solid waste otherwise follow the current regulations about demolition 1 6 Labelling Each device has got an identifying label positioned on the device itse...

Страница 3: ...ate of use date of checks name of users any comments When the device is being used the assistance of qualified staff must be guaranteed Do not store the device underneath any heavy objects which could cause structural damage Store in a cool dry dark place and do not expose to direct sun Store and transport device in its original packaging The device not be exposed to or come into contact with any ...

Страница 4: ...atomy In determining the load of the total weight on the product the operator must consider the weight of the patient the equipment and the accessories Moreover the operator must consider that the overall dimensions of the patient do not reduce the functionality of the device Never leave the patient unassisted on the device because he may be injured The device and all its components after washing ...

Страница 5: ...s not present any contraindications or collateral effects 2 4 Physical requirements of the operators Spencer 480 stretcher is destined to professional use only The rescue operators must have the following minimum requirements physical capacity for operating the device be able to seize the device firmly with both hands have strong back arms and legs for lifting pushing and pulling the stretcher hav...

Страница 6: ...al Devices MDD 2007 47 CEE Modifications to 90 385 CEE Directive about active implants Directive 93 42 CEE about medical devices and Directive 98 8 CE about the introduction of biocides onto the market Legislative Decree 24 02 1997 n 46 Application of the 93 42 CEE Directive about Medical Devices Legislative Decree 25 01 2010 n 35 Modifications and additions to the 20 02 97 Decree n 46 UNI EN ISO ...

Страница 7: ...from direct sunlight It must not be placed in contact with any substances or chemical agents which could cause damage and reduce safety characteristics During storage do not place heavy materials over the device The chair should not be considered and used as a shelf for any type of material 4 2 Preparation On receipt of the product Remove the packaging and display the material so that all componen...

Страница 8: ...e safety devices have not been removed Ensure after proper lubrication if the problem persists If so put the device out of service and contact the service centre Difficulties in the extraction and insertion of telescopic handles Sediments in the sliding site or yielding of the aluminium profile Carry out thorough cleaning If the problem persists do not use the device for handling involving the asc...

Страница 9: ...parts accessories that are either original or approved by the supplier in such a way that each operation causes no alteration or modification to the appliance Possession of the checklist of operations carried out on the appliance Guarantee complete adherence to the instructions of the Directive 93 42 CEE which includes also the obligation towards the Manufacturer to maintain post sales records and...

Страница 10: ...horised centre we have to underline that a report regarding all operations carried out must be requested This will permit both Spencer Italia S r l and the end user to keep a log book regarding the operations carried out on the device 5 2 2 Special servicing Only the Manufacturer or centres with written authorisation are authorised to complete any special servicing operations For any operations th...

Страница 11: ...y having attended specific training for this device and not for similar products Keep this document at least 10 years from the end of life of the device Operator s name Training date Training method user s manual during service former class etc Trainer Basic training Advanced training ...

Страница 12: ...be modified without any warning and is not to be intended as a commitment on behalf of Spencer Italia S r l Spencer products are exported to many countries and the same identical regulations are not always valid For this reason there could be differences between the description here described and the product actually delivered Spencer continually strives to reach the perfection of all items sold W...

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