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Summary of Contents for GERATHERM Bodystik
- Page 1 Bodystik User Manual Version 1.2.2 Date 17th October, 2014...
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Page 2: Table Of Contents
2.2.4 Flow sensor installation ............9 2.2.5 Cabin connections ............... 10 2.2.6 Cabin controls ..............11 2.2.7 Power on the Bodystik ............12 Security................12 2.3.1 General Security information ..........12 2.3.1.1 Norms and Guidelines ............13 2.3.1.2 Electromagnetic compatibility ..........13 2.3.2... -
Page 3: Welcome To Blue Cherry
The copyright for Blue Cherry is owned by Geratherm Respiratory. Permission is given to use the Blue Cherry software provided on the installation CD upon acceptance of the EULA. (see appendix) Blue Cherry™... -
Page 4: Bodystik
USB interface. The established Ergoflow Flow sensor Principle is used for flow measurement. The Bodystik can only be used together with the tool and gear wagon authorized by Geratherm Respiratory. The galvanic isolation of the electric power system is done by the tool and gear wagon. All... - Page 5 It is possible for the user to manually adjust almost every curve. The main application of the Bodystik is the lung function diagnostic plus its use in clinical areas. The standard scope of supply for the Bodystik includes the following...
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Page 6: Setup
It is recommended to the operator to perform all described methods to clean, setup, sterilize and disinfect the device. Before testing with the Bodystik multiple components have to be connected with each other as well as the USB connection has to be established. -
Page 7: Shutter Unit
User Manual Bodystik Connection panel at the bottom of the stand: Compressed air connection for gas supply (1), sample gas connection (2), electric unit connection (3). 2.2.2 Shutter Unit Now move the shutter (1) as far as it will go into the closing head (2). -
Page 8: Installation Of Demand Valve (Only Option Co Diffusion)
2.2.3 Installation of demand valve (only option CO Diffusion) If the Bodystik includes the option CO Diffusion the demand valve has to be connected additionally. Therefore move the demand valve (1) as far as it will go into the closing head, just like shown in picture (2). -
Page 9: Flow Sensor Installation
User Manual Bodystik Ensure that all connections are connected accurately and without too much power. The gas supply hose should only be connected to gas bottles with the following content: up to 0.3% CH4 up to 0.3% CO up to 0.3% C2H2 (optionally) -
Page 10: Cabin Connections
Cabin connections Connect the provided power supply to the jack of the Bodystik. Now connect the Bodystik via the provided USB cable to a free USB port at your computer. Connection panel of the Bodystik: power supply jack (1), USB port (2),... -
Page 11: Cabin Controls
User Manual Bodystik 2.2.6 Cabin controls The following controls, which were shown below, are arranged out of the cabin: Emergency stop switch (1), door status LED (2) glows green if door is closed, door opener (3), push-button stand up (4), push-button stand... -
Page 12: Power On The Bodystik
Power on the Bodystik First connect the power supply to an unused jack of the multiple socket outlet of the medical cart. By using the switch of the medical cart you can turn the Bodystik power supply on or off. Security 2.3.1... -
Page 13: Norms And Guidelines
Strong radio transmitters should not be used close to the device. Do not use mobile phones and cordless phones close to the device. There may be an influence to medical devices. The interference resistance is 3V/m. Do not use a higher level close to the Bodystik. BODYSTIK_MAN_ENG_V1.2.2_REV01.DOCX Page 13... -
Page 14: Secure Use Of Bodystik
2.3.2 Secure use of Bodystik The Bodystik is a medical device to perform PFT measurements. It is highly recommend that the user observes all warning notices in order to ensure a safe use of the device. Following parts of the device are... - Page 15 Remove excess fluids using a dry cloth. A surface and/or wisp disinfection is designated for the Bodystik. Please attend to the additional details in the chapter Disinfection. The device should not be exposed to rain or other humidity and should not be operated in wet environments.
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Page 16: Cleaning And Disinfecting The Flow Sensor And Shutter
User Manual Bodystik The device should not be used in dirty environments. By the time the door is open never apply pressure from above to the door. It is then possible that the cabin is tilting forward. Please advise the patient of the possibility to open the door from inside the cabin by using the switch. - Page 17 User Manual Bodystik Always ensure all connections and cables are connected properly. All additionally connected devices must comply with legal regulations and the total leakage current must not exceed the maximum allowed valued specified in the Norm DIN EN 60601-1.
- Page 18 User Manual Bodystik Situation Medical used room Non-medical Possible Within patient Out of used room solution area patient area resource A and B within patient area IEC 60601 IEC 60601 resource A and B for B: additional within patient area...
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Page 19: Disposal
User Manual Bodystik 2.3.5 Disposal The described device contains electronic components, which must not be disposed of with domestic waste. Always ensure disposal is carried out in accordance with local directives. 2.3.6 Product Labelling Example of typical product labelling: SN: designates the serial number for the device. -
Page 20: Used Symbols
Separate collection of electro and electronic devices IPX0 Indicates no protection against dripping water Manufactured according RoHS directive 2002/95/EC Geratherm Respiratory devices carry this CE no according to directive 93/42 ECC for medical devices and fulfil the requirements of annex II 0494 of the directive BODYSTIK_MAN_ENG_V1.2.2_REV01.DOCX... -
Page 21: Maintenance
User Manual Bodystik Maintenance The Bodystik has been designed to ensure it is a low maintenance device. Only minor maintenance is required to ensure trouble free operation. Interval Maintenance work Once a day Flow sensor, flow sensor housing and shutter unit cleaning... -
Page 22: Warranty
Geratherm Respiratory, and respectively equal to installation date if purchased from a sales partner. All service must be provided by Geratherm Respiratory or an authorized service partner of Geratherm Respiratory. Geratherm Respiratory will not accept warranty claims on any unauthorised repairs. -
Page 23: Technical Data Bodystik
User Manual Bodystik Technical Data Bodystik Modifications are not permitted with this device Technical Data: Dimensions: 750 mm x 850mm x 1700mm (L x w x h) Weight: 140 kg Electrical data: IP protection type: IPX0 IEC 529 Protection class: Classification according to MDD: IIa 93/42/EWG date 14.06.93 Appendix IX...
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