Famed FREYA 3 Instruction Manual Download Page 11

Instruction Manual for the Delivery Table FREYA 3 

Page 11 

2. 

Transport and commissioning 

2.1. 

Transport 

The  product  may  be  transported  by  all  publicly  available,  covered  means  of  transport.  During 
transport, the device should be secured against moisture and immobilised. 

The device should be transported under the following conditions: 

-

 

temperature: 

 –10°C to 60°C  

-

 

relative humidity:  

 20% to 80% 

While  transporting,  storing  and  unpacking  the  device,  the  temperature  fluctuation  may  not  exceed 
10°C  within  an  hour.  The  device  may  be  unpacked  onl y  after  reaching  the  room  temperature  where 
the device is kept. 

Having transported the device to the building  where it will be mounted,  leave it for at least 12 hours. 
Only then can you proceed to commissioning. 

It is acceptable to stack the device in layers  acc. to the package marking. In case of absence  of the 
marking, the layer stacking is forbidden. 

In the event of transporting the device under different conditions, especially in low temperatures, it is 
necessary  to  consult  with  the  manufacturer  as  regards  the  transport  method  and  package  type 
ensuring safe transport. 

2.2. 

Unpacking and first start-up 

 

NOTE! 

If the device is mounted by the service team of FAMED 

ś

YWIEC Sp. z o.o., then the 

user is exempt from performing the activities described at this point. 

The  delivery  table  supplied  by  the  manufacturer  is  pre-installed,  in  a  box  with  these  dimensions: 
length:~  69 in  (1,750 mm)  x  width:~47 in  (1,200 mm)  x  height:~43 in  (1,100 mm)  and  weight:  ~38 st 
(240 kg).  
So as to avoid damage of the device, unpack and mount it in the building. 

So as to prepare the table for work after its delivery or transport: 

-

 

carefully acquaint yourself with the instruction manual, 

-

 

remove the package, 

-

 

remove the materials protecting the table while in transport, 

 

NOTE! 

Packages may have the following signs: 

 

reusable package 

 

recyclable package 

 -

 LDPE package 

Handling  of  packaging  waste  should  meet  legal  requirements  specific  to  the 
environmental  protection,  applicable  where  the  product  enters  the  market  in  the 
packaging. 
Packaging  waste  consists  of  recyclable  materials  that  should  be  appropriately 
segregated  and  submitted  to  the  local  segregated  waste  collection  site  in 
accordance with requirements of the local legislation.  

Reusable packaging should be returned to the medical device supplier.

 

Summary of Contents for FREYA 3

Page 1: ...INSTRUCTION MANUAL Delivery table type LM 03 FREYA 3 Serial no Revision 2 00 Publication date 26 03 2015 FAMED YWIEC Sp z o o Annexes 2 3 4 Index of Spare Parts...

Page 2: ...e essential requirements contained in Annex I to the directive and Act on medical devices The compliance procedure has been performed acc to Annex VII to the directive Manufacturer FAMED YWIEC Sp z o...

Page 3: ...ranty null and void Before any repairs disconnect the device from the mains Safety notes Below is the warning Warning Follow the instructions for safe use This warning can be found on parts and mechan...

Page 4: ...ly exercise caution while adjusting the extended lying surface in relation to the permanent one as the distance between the permanent frame and the extended one is too small if the pressure knob is us...

Page 5: ...r underneath must be free of obstacles During the table movement avoid collisions Exercise caution while removing and mounting the permanent lying surface moulding Application of excessive force may l...

Page 6: ...8 ARMCHAIR POSITION OF THE DELIVERY TABLE CARDIAC CHAIR 18 3 9 QUICK LEVELLING OF THE THIGH AND BACKREST SECTIONS CPR FUNCTION 18 3 10 POSITION 0 18 3 11 EXTENDED LYING SURFACE FRAME POSITION ADJUSTME...

Page 7: ...used The user is obliged to ensure that the device is operated in compliance with its intended purpose and that it is operated under appropriate conditions in a manner pursuant to this instruction man...

Page 8: ...nel with the option of locking the respective electrical functions of the delivery table Control panel in the side rail Wired controller Foot controllers option 9 Backlight lamp from underneath the de...

Page 9: ...related to the structure technology and materials without compromising the technical utility parameters and safety of the device 1 7 Safety The device structure ensures safe operation and use provide...

Page 10: ...nvironment is described in which the medical device Delivery Table LM 03 should be operated The user should observe the guidelines and warnings included in the tables NOTE The use of accessories addit...

Page 11: ...ransport method and package type ensuring safe transport 2 2 Unpacking and first start up NOTE If the device is mounted by the service team of FAMED YWIEC Sp z o o then the user is exempt from perform...

Page 12: ...r the electronic table control system works performing all the functional table movements by use of all the available control elements foot controller and side panels Furthermore check whether the loc...

Page 13: ...elected functions so as to prevent the patient from their activation with the wired controller or the ones in the side rails The central control panel enables the control of the following delivery tab...

Page 14: ...at the same time inclination angle of the backrest and thigh sections AUTOCONTOUR Trendelenburg and reverse Trendelenburg angles The table controller without the central control panel or locking pane...

Page 15: ...with control panels on the outer side see Fig 2a whereas on the inner side with control panels see Fig 2b which enable the activation of the table functions by the patient and medical staff as describ...

Page 16: ...e Trendelenburg when you lower the lying surface to the min height or during the Trendelenburg position marking compliant with pt 8 2 3 3 Backrest section angular position adjustment with the CPR func...

Page 17: ...central panel are marked with the symbol Angular couch position can be changed only by medical personnel The Trendelenburg position is a rescue position NOTE Do not lay any objects on the plastic base...

Page 18: ...e patient s head and push the backrest section down So as to level the thigh section pull the lever under the shank section and push the thigh section down 3 10 Position 0 The position 0 of the delive...

Page 19: ...e between the mounting element of the hand holder and the side rail Failure to observe the above note may at the extreme angles lead to crushing the patient s operator s fingers or to damaging the del...

Page 20: ...r underneath must be free of obstacles During the table movement avoid collisions Do not roll the delivery table across electrical cables 3 15 Use of the side rails Fig 4 The side rails fig 4 are atta...

Page 21: ...ht be damaged Application of excessive force might result in damaging the mouldings 3 17 Infusion rod The infusion rod is embedded in bushings located in the permanent lying surface frame near the hea...

Page 22: ...ually with the agents recommended in annex 2 to this instruction manual NOTE Use foil underlays for spots exposed to preparations applied during various procedures The contact with preparations for di...

Page 23: ...Instruction Manual for the Delivery Table FREYA 3 Page 23 4 Utility parameters The schematic figure below presents the most important utility functions of the delivery table and their marking...

Page 24: ...tion contained herein do not operate it Consult with the manufacturer supplier dealer Using the defective device may lead to damage sustained by the user for which the manufacturer assumes no liabilit...

Page 25: ...rotection NOTE The device contains products which may pose a threat to the environment gel battery type EP 1 2 12 2 pcs Rules of conduct as regards worn products that may pose a threat to the environm...

Page 26: ...should be settled acc to pt 6 6 Troubleshooting So as to ensure safe and reliable functioning within the device lifetime the user shall perform inspections as regards the compliance with standard IEC...

Page 27: ...pply cable disconnected controller defective control system or actuator connect the controller notify an authorised service centre seat section angle adjustment actuator will not work disconnected pow...

Page 28: ...ng features The user is to ensure that the medical device Delivery Table LM 03 is used in this type of environment Resistance IEC 60601 1 2 Test level Resistance level Explanations and guidelines Elec...

Page 29: ...a should be lower than the column resistance level within the entire frequency range b There might be interference in the medical device functioning if the column is being used in the vicinity of equ...

Page 30: ...ective identification plate areas 1 Logo symbol manufacturer production date manufacturer name and address 2 Device symbol 3 General marking CE marking Warning Follow the instructions for safe use Not...

Page 31: ...t 215 kg 39 st 250 kg 6 Maximum load of the extended lying surface frame 27 st 170 kg 7 Note For cleaning washing and disinfecting do not use agents which contain active oxygen or chlorine 8 Infusion...

Page 32: ...st inclination adjustment pedal option 18 Seat inclination adjustment pedal option 19 Warning Follow the instructions for safe use 20 Follow the instructions Note The manufacturer reserves the right t...

Page 33: ...00 3 Famed ywiec Sp z o o 6 Extension cover 1 C220920000003 B00 3 Famed ywiec Sp z o o 7 Lying surface mattress 1 C220920100000 A00 3 Famed ywiec Sp z o o 8 Extension mattress 1 C220920110000 3 Famed...

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