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USER GUIDE // 

PEDIATRIC IMMOBILIZATION SYSTEM PA-190 

Review 2021/09

 

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21.    Attention:  laboratory  testing,  post  production  tests  and  instruction  manuals 
cannot  always  consider every possible scenario for use. This means that in some 
cases  the  performance  of  the  product  could  be  notable  different  from  results  to 
date  obtained.  Instructions  are  continually  being  updated  and  are  under  tight 
surveillance of fully qualified staffs with adequate technical formation.

 

 

22.  Both public and  private operators are obliged to report  any  accident  involving 
any medical device to the Ministry of Health and the manufacturer as specified and 
within the time given by European regulations.

 

 

23. Both public and private operators are obliged to inform the manufacturer of the 
measures to be taken to guarantee the safety and health of patients and users of 
any medical device.

 

 

24. As a distributor or end user of the products manufactured and/or distributed by 
Promeba, S.L., you are strictly obliged to know the legal provisions in force in the 
country  of  destination  of  the  goods,  applicable  to  the  devices  to  be  supplied 
(including  the  regulations  relating  to  technical  specifications  and/or  safety 
requirements)  and,  therefore,  understand  the  necessary  requirements  to  ensure 
compliance  of  the  products  themselves  with  all  the  legal  requirements  of  the 
territory.

 

 

25.    Promptly  notify  PROMEBA  regarding  any  revisions  to  be  made  by 
manufacturer in order to guarantee the  conformity  of  the  product  to  the  territory

’s 

legal  specifications  (including  those  resulting  from  rules  and/or  norms  of  other 
nature).

 

 

26.  Act  with  all  due  care  and  diligence,  and  contribute  to  ensure  conformity  to 
general  safety  requirements  of  all  devices  marketed  in  the  territory,  by  providing 
final  users  with  all  necessary  information  for  carrying  out  periodical  checks  on 
their devices, as specified in the relevant user manual.

 

 

27.  Actively  contribute  to  product  safety  checks  on  products  sold,  by 
communicating any relevant risk analysis information both to the manufacturer and 
to any competent authorities so that the necessary actions can be promptly taken.

 

 

28.  Be  aware  that  in  the  event  of  any  failure  to  conform  to  the  above  mentioned 
requirements  you  will  be  deemed  fully  responsible  for  all  damages  that  might 
occur.  Therefore  we  expressly  disclaim  any  responsibility  and/or  liability  for  your 
non-compliance with the present 

“Regulatory provisions”.

 

Summary of Contents for PA-190

Page 1: ...USER GUIDE PEDIATRIC IMMOBILIZATION SYSTEM PA 190 Review 2021 09...

Page 2: ......

Page 3: ...ents of the operators 06 01 8 Intended purpose 06 01 9 General warnings 06 01 10 Specific warnings 09 01 11 Residual risk 09 01 12 Reference standards 10 01 13 Life span 10 02 PRODUCT DESCPRIPTION 10...

Page 4: ......

Page 5: ...manufacturer s serial number to identify a specific medical device Indicates the manufacturing date The symbol must be accompanied by a manufacturing Date yyyy mm adjacent to the symbol It is placed t...

Page 6: ...nts of the operators Promeba s Pediatric immobilization system PA 190 is destined to professional use only The operators must be trained in efficient effective and safe patient transport 01 8 Intended...

Page 7: ...other than described in this manual is forbidden 10 Do not alter or modify in any way the device any such interference could cause malfunctions and injury to the patient and or rescuer 11 The device m...

Page 8: ...cluding the regulations relating to technical specifications and or safety requirements and therefore understand the necessary requirements to ensure compliance of the products themselves with all the...

Page 9: ...ect the product Use a hydroalcoholic based disinfectant and wash with water 5 The device and all its components after washing should be allowed to dry completely before storing 6 Keep clean as routine...

Page 10: ...d and authorized internal and external technicians In case these annual checks are not carried out the device must be disposed of according to the information in paragraph 01 4 and the manufacturer mu...

Page 11: ...Open the head support 7 Align the color coded restraints with the patients as follows Restraint Colour coded Area Chest restraint Red Even with patient s armpits Upper hip restraint Yellow Just above...

Page 12: ...e the patient s chin if needed 13 Wrap the head support around the patient s head The slots in the head support should be in line with the patient s ears 02 3 3 Transport the Patient 1 Use an ambulanc...

Page 13: ...t the backboard into the cover and close the cover flap 4 Attach the head support and the Pediatric Immobilization System and fasten the restraints 5 Slide the Pediatric Immobilization System into its...

Page 14: ...E REGISTER The product must be used by trained personnel only having attended specific training for this device and not for similar products Keep this document at least 10 years from the end of life o...

Page 15: ...as indicated by the manufacturer in this user s manual Keep this document at least 10 years from the end of life of the device DATE TYPE OF SERVICE Maintenance verification extension of useful life OP...

Page 16: ...t The possession of this document does not entitle no license to these patents The information contained in this document does not affect or change the specifications or product specifications or warr...

Page 17: ...product or incorrect installation of accessory parts not previously tested iii States or defects of the system in which the product is used or incorporated with the exception of other pro ducts Prome...

Page 18: ...ta o la inexactitud de la informaci n aqu mencionada All rights reserved Variations can be done without notice Promeba S L is to be considered not responsible for damages caused by the lack or the wro...

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