Penlon prima sp service manual

Be the first to ask a question! The Penlon Prima SP2 is an anesthesia system designed for use on patients in need of anesthetic gas circulation. The primary use cases for the system are the anesthetic application to patients of all ages and needs. The device features a large rectangular color touchscreen, six ventilation modes, and the ability to use up to four different types of gas.

InterMed Penlon designed and produces the device. Penlon has been producing respiratory health equipment since , originally as Longworth Scientific Instrument Company Limited. The company has been operating under Penlon since , and has since acquired various other firms related to respiratory health devices.

Joined: Jun Could you send them all to me? Hi Piter: Can you sahre with me, too? Can you send it to me too? Thanks in advance!! Jorge biometuy gmail. May you send it to me?? Thanks a lot lm gmail. Dear Piter Can you send it to me too? Mohammed mewais gmail. Joined: Jan Hello Piter , Is possible please to have a copy? Thank you very much for your support and attention. Ed SWM. Hi Piter, Would you be kind enough to email me a copy?

Best regards Ed. Geoff Hannis. Or better yet, why not post it to Frank's website? That way anyone who needs it will be able to download. That goes for all good people ready to donate. Thanks i need the service manual please my email: eng. Joined: Jul Hi Piter Could you send me service manuals of all penlon ventilators please? My e-mail is erenarikan gmail.

Joined: Oct Is possible please to have a copy? Thank you very much best regards. Hi Piter Will you share with me? Thank you. Joined: May Guadalajara Jalisco Mexico. Diego de Jesus Gonzalez Beltran. Hi Piter can yo0u mail them to me also at: info southwestmedical. On models with spirometry, care must be taken to ensure that the flow sensors are connected correctly to the inspiratory and expiratory ports of the absorber.

The Vent Inop ventilator inoperative alarm indicates that one of the following conditions has occurred:. A The drive gas solenoid has failed. B The flow control valve has failed. C Internal electronic fault. D Internal electrical fault. Note that if a ventilator error is detected, an error code will be displayed on the front control panel display. The ventilator is designed to be used with a distal sensing tee only. Catalogue No.

It is important that the distal sensing tee is properly located in the expiratory limb of the circuit between the patient and the expiratory one way valve. The patient must be continuously attended and monitored when Patient Support Mode is in use. Opening the control unit by unauthorised personnel automatically voids all warranties and specifications.

If the control unit seal is broken, the manufacturer assumes no liability for any malfunction or failure of the ventilator. For continued protection against fire hazards, replace the two fuses only with the identical type and rating of fuse. If the internal battery is fully discharged, the ventilator will not function in the event of mains power failure. The battery must be recharged before the ventilator is used clinically, otherwise backup cannot be guaranteed.

Used or defective batteries must be disposed of according to hospital, local, state, and federal regulations. No oil, grease or other flammable lubricant or sealant must be used on any part of the ventilator in close proximity to medical gas distribution components.

Exterior panels must not be removed by unauthorised personnel and the apparatus must not be operated with such panels missing. The valve seat on the patient gas exhalation diaphragm valve in the base of the bellows assembly must be cleaned regularly - see section 7. Failure to keep the valve seat clean could result in the diaphragm sticking, thus preventing exhalation. Great care must be taken not to damage the precision surface of the valve seat on the patient gas exhalation diaphragm valve in the base of the bellows assembly.

Never use any hard object or abrasive detergent to clean it; use only a soft cloth. If the valve seat is damaged, the valve will leak and may cause serious ventilator malfunction. Do not sterilise the ventilator control unit. The internal components are not compatible with sterilisation techniques and damage may result. For ventilator components which require. See sections 7. Those parts suitable for ethylene oxide sterilisation should, following sterilisation, be quarantined in a well ventilated area to allow dissipation of residual gas absorbed by the components.

The exhalation valve located in the bellows base assembly and the paediatric bellows adaptor must be cleaned and sterilised separately. Care must be taken not to let any liquid run into the control unit; serious damage may result. Always check for correct fitment, and carry out a full function test before clinical use, if the bellows has been removed and refitted for any reason.

See sections 5. Damage may occur to the battery if it is allowed to remain in a discharged state. Check the battery frequently if the ventilator is in storage see Appendix 1. On models with spirometry, fresh gas compensation is disabled if :. On models with spirometry, fresh gas mixture compensation is disabled if :.

We recommend calibration of the oxygen monitor every time the system is turned on, as a safety precaution. Do not attempt to open the fuel cell.

The sensor contains small quantities of :. Used or defective cells must be disposed of according to hospital, local, state, and federal regulations. See section 3. Once exhausted, the sensor must be disposed of according to hospital, local, state and federal regulations.

The sensor measures oxygen partial pressure, and its output will rise and fall due to pressure change. Do not sterilise the oxygen sensor or control unit components. These components are not compatible with sterilisation techniques and damage may result. Do not autoclave or expose the sensor to high temperatures. If the sensor shows signs of being affected by condensation, dry the sensor with soft tissue.

To maintain maximum sensor life, always remove the unit from the breathing circuit after use. The accuracy of flow and volume measurements may be reduced if the oxygen monitor is not in use. Fresh gas mixture compensation is disabled if the oxygen monitor is switched OFF.

The AV Ventilator is a software controlled, multi-mode ventilator, designed for mechanical ventilation of adult and paediatric patients under general anaesthesia. In addition, in spontaneous mode, it can be used to monitor spontaneously breathing patients. It is designed for use in closed-circuit anaesthesia and also to drive a Mapleson D circuit. The AV Ventilator is intended to provide continuous mechanical ventilatory support during anaesthesia.

The ventilator is a restricted medical device intended for use by qualified trained personnel under the direction of a physician. Specifically the ventilator is applicable for adult and paediatric patients. The ventilator is intended for use by health care providers, i. Physicians, Nurses and Technicians with patients during general anaesthesia.

The Oxygen Monitor is intended to continuously measure and display the concentration of oxygen in breathing gas mixtures used in anaesthesia, and is intended for adult and paediatric patients. The oxygen monitor is a module within an anaesthesia machine, and is a mandatory module when the spirometry option for AV is specified.

The oxygen monitor is intended for use by health care providers, i. Physicians, Nurses and Technicians for use with patients during general anaesthesia. In addition, models with spirometry are fresh gas compensated and also feature user selectable gas mixture compensation.

The print function provides a permanent record of function activity for up to eight hours during a procedure, or can be used to record waveforms. The bellows unit can be easily detached and then refitted to the bellows base assembly to facilitate cleaning.

The ventilator drive gas supply can be oxygen or air. The supply must be at to kPa 38 to psi. Note that the drive gas is specified by the customer prior to delivery.

Conversion from one drive gas to another must be carried out by a Penlontrained service engineer. Note that on models without spirometry, the patient support function is disabled. RS Port. Connect to cylinder or pipeline supply. Drive gas pressure builds up above the bellows, which starts to move down, forcing patient gas into the breathing system. The exhaust valve opens, allowing the drive gas above the bellows to escape to atmosphere.

The bellows exhalation diaphragm valve in the base of the bellows assembly opens when the bellows reaches the top of the chamber. Patient circuit gas exits through the bellows assembly exhaust port, and then through the ventilator exhaust valve. Fresh gas flows in the patient circuit. Pressure in the bellows increases.

The PEEP proportioning valve will maintain the pressure with a controlled bleed flow. The drive gas is filtered with a micron Input Gas Filter which protects the pneumatic components from incoming particulate matter. The Low Supply Pressure Detector is a pressure switch set at a predetermined level to detect a loss or reduction of the input gas source pressure.

The Inspiratory Valve is an electro- pneumatically-driven valve with a large orifice. The Drive Gas Flow Metering Valve is a variable-orifice needle valve which determines the drive gas flow rate to the bellows during inspiration. The Valve Position Feedback Potentiometer and the Flow Control Motor function together to set a flow rate as required by the front panel controls.

The flow then closes the exhalation diaphragm valve and pushes the bellows downward. At the end of inspiration the exhaust valve opens and allows the drive gas in the top of the bellows housing to exhaust out through the Exhaust Outlet.

They hope to resolve this issue by the end of the However they are IHE compliant and forward compatible right now. By the way do you have an evaluation checklist or sheet in excel or word, it would really be handy for eval purposes. Its taking more time than I expected for these evals to proceed. Thank you again for all your suggestions and input. It really means a lot to me Hi Tim, Just wondedring if you are any further ahead yet?

Regards Mick. Who's Online Now 0 members , guests, and 67 robots. Key: Admin , Global Mod , Mod. Most Online 5, Jan 29th, Powered by UBB. Forums Calendar Active Threads. Previous Thread. Next Thread. Print Thread. Copy Link to Clipboard. Share Post on Facebook. Share Post on Twitter. Share Post on Reddit. Joined: Oct Posts: 3 warwickshire Mick Newbie.

Mick Newbie Joined: Oct Posts: 3 warwickshire. Switch to Threaded Mode.