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USER GUIDE // 

ROLLED SPLINT PA-08 

Review 2021/09

 

 

 

 

 

02.2 Technical parameters

 

Model 

PA-08 

Unfolded size 

0.9*0.11 cm 

N.W. 

0.4 KG. 

Packing 

QTY 

60 pcs/CTN 

Size 

46*37*37 cm 

G.W. 

10 kg. 

 

02.3 Use Method 

1. Determine the position that needs to be fixed, unfold the splint, and initially shape the shape that conforms to 
the human body part according to the needs of the part. 
 
2. Attach the splint to the desired area and secure it securely. 
 

Very important: 

 
-  The  operator  must  read  this  manual  carefully  and  follow  the  instructions  to  become  familiar  with  the  correct 
operation  and  maintenance  of  the  splint.  Otherwise,  the  company  will  not  be  responsible  for  the  dangerous 
accidents. 
 
-  If  the  patient  has  any  problems  in  use,  they  are  not  allowed  to  adjust  themselves  and  need  to  inform  the 
professional. 
 

 

03. 

OPERATION 

 

 

03.1. Transport  

1. Be transferred by common transporting tools: plane, ship or road. 
 
 
 
 
 
 
 
 
 
2. The Rolled splint PA-08 can be manually handling 
 
3. The Rolled splint PA-08 should be kept away from cutter or sharp objects in order to avoid damage. 
 
4. At

tachments: certificate, user’s manual. 

 

 

03.2. Storage  

1. Store this Rolled splint, in the place of damp proof and non-corrosion environment. 
 

Summary of Contents for ROLLED SPLINT PA-08

Page 1: ...USER GUIDE ROLLED SPLINT PA 08 Review 2021 09...

Page 2: ......

Page 3: ...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 02 1...

Page 4: ......

Page 5: ...rer 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 to inform...

Page 6: ...cations or collateral effects 01 7 Physical requirements of the operators Promeba s Rolled splint PA 08 is destined to professional use only 01 8 Intended purpose Mainly used in hospitals ambulances s...

Page 7: ...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 must not in...

Page 8: ...e 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 req...

Page 9: ...because he may be injured 4 Do not use bleach to disinfect the product Use a hydroalcoholic based disinfectant and wash with water 5 The device and all its components after washing should be allowed...

Page 10: ...cturer which uses specialized 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...

Page 11: ...ly and follow the instructions to become familiar with the correct operation and maintenance of the splint Otherwise the company will not be responsible for the dangerous accidents If the patient has...

Page 12: ...ortation as shown by the box stacking 03 3 Maintenance 1 Inappropriate use and lack of maintenance can cause damage to people and objects 2 It is recommended that you check the surface of the Rolled s...

Page 13: ...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 of the devi...

Page 14: ...ted 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 OPERATIONS...

Page 15: ...ession 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 warranties of...

Page 16: ...r 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 Promeba S L des...

Page 17: ...os causados por la falta 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...

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