INJECTOMAT AGILIA SERVICE MANUAL PDF

Embed Size px x x x x Drug library Volume Limit Syringe list

Author:Grosho Shat
Country:Comoros
Language:English (Spanish)
Genre:Politics
Published (Last):10 September 2017
Pages:46
PDF File Size:14.13 Mb
ePub File Size:5.48 Mb
ISBN:316-4-90127-492-6
Downloads:47550
Price:Free* [*Free Regsitration Required]
Uploader:Shacage



Thank you for interesting in our services. We are a non-profit group that run this website to share documents. We need your help to maintenance this website. Please help us to share our service with your friends. Share Embed Donate. Injectomat Agilia has a range of flow rates from 0. It is the ideal device for intensive care units and neonatology. Injectomat Agilia is fitted at the back with an infrared cell. Injectomat Agilia is equipped with an integrated system allowing it to be fixed onto a pole or a rail.

Its integrated locking system allows three Agilia IV pumps to be stacked on top of one another to facilitate transportation. Operation diagram Supply Mode, battery management, battery life indication Introduction Precautions for use Fresenius Kabi recommend a complete reading of the Instructions For Use manual, in accordance with norm EN 60 Fresenius Kabi cannot, in any circumstances, be held responsible for any medical or other problem due to incorrect use of the device.

Kindly consult the Instructions For Use manual for more details. Atmospheric pressure: hPa to hPa. Operation safety As soon as it is in operation, the Injectomat Agilia syringe pump ensures continuous surveillance of its functions.

Any internal fault or any procedural anomaly is immediately detected. Nevertheless, abnormal functioning of the device, without a defined cause, must always be brought to the attention of the qualified staff in your establishment or our Technical Service. The alarm for the most rapidly detected discrepancy is activated. Injectomat Agilia is equipped with an internal battery that ensures normal functioning during a mains power cut.

In addition, a safety fuse protects the concerned mains area. Protection against leakage current: Defibrillation-proof type CF applied Protection against electric shocks: class II. Functional earth. Description and operation Physical description Flanges groove Plunger protection Cover Plunger disengagement control Angle bracket Plunger Base Syringe clamp Control panel Injectomat Agilia is made up of three main parts: a base, a cover and an angle bracket.

The cover contains: a display board. The base contains: a CPU board a mechanical framework assembly a plunger unit. The angle bracket contains: a power supply board and a battery Fixing clamp system.

Preventive maintenance Recommendations The device can only be checked, serviced or repaired by Fresenius Kabi or by a certified and approved maintenance service. Any abnormal functioning of the pump must be brought to the attention of your in house qualified technical personnel or our Technical Service.

Should you need to return the pump to our Technical Service, it should be cleaned, disinfected and very carefully packaged, preferably in its original packaging, before being shipped.

For all information concerning the repair and use of the pump, kindly contact our Technical Service or our Customer service. Fresenius Kabi is not liable for loss or damage to the pump during its transport to our Technical Service.

This procedure, which includes battery replacement, should be carried out by a qualified technician. Any abnormal functioning or failure must be reported to the qualified technical staff in your organisation or to our Technical Service.

In these instances, the pump should not be used. Important: If these maintenance procedures are not observed, the pump correct operation will be impaired. Quality control At the request of the health organisation, a quality check will be carried out every 12 months. A quality check not included in the guarantee consists of different inspection procedures as defined in the pump Technical Manual. Only a qualified technician may perform the quality check which must be performed using Fresenius Kabi software.

For more information, kindly contact our Technical Service. Recycling of obsolete batteries and devices : Before disposal, remove battery from the device. Batteries and devices with this label must not be disposed of with the general waste.

They must be collected separately and disposed of according to local regulations. For further information pertaining to waste processing regulation, contact your local Fresenius Kabi. Preventive maintenance Checks A quality control certificate is available at the end of this section.

In order to ensure the smooth running of the checking procedure, recharge the battery for 16 hours beforehand. Keyboard description. Key Function ON switches on the pump. OFF switches it off when pressed for over three seconds. The selection keys scroll through the numbers and letters on the tenths, units and tens values and allow one to move to the next menu. OK validates your test selection or moves the cursor. It is advisable to clean and disinfect the device external surfaces regularly and especially before connecting a new patient and before any maintenance operation in order to protect patient and staff.

Disconnect the device from its main supply before cleaning. Do not let liquids enter the device housing. If the device is placed in a high contamination risk unit, it is advisable to leave it in the room during disinfecting, after having disinfected it with amoist cloth. Avoid abrasive scrubbing which could scratch the casing.

Do not rinse or wipe the surfaces. These aggressive agents could damage plastic parts and cause device malfunction.

They lead to tarnishing and small cracks in the plastic, and do not provide the necessary cleaning prior to disinfection. Disinfecting SPRAYS may be used, in accordance wih the manufacturer recommendation, from a distance of 30cm of the device, avoid the accumulation of the product in liquid form.

Please contact the appropriate service responsible for cleaning and disinfecting products in your establishment for further details. Storage The device should be stored in a dry, cool place. In case of prolonged storage, the battery should be disconnected via the battery access flap situated underneath the device. This should be done by a qualified technician. Fully recharge the battery before using the device to avoid any risks caused by micro power Use of the internal battery This device is provided with NiMH battery.

When the device is disconnected from the mains, it automatically switches to battery mode. Before starting for the first time, charge the battery for approx. In case of frequent mains operations, battery life may be decreased. To limit this risk, it is recommended to use the device on the battery mode, approximately every 4 weeks, until getting a battery pre-alarm signal. Diagnostic Troubleshooting guide Problem Cause Action End of infusion detected too early at approximately 10ml.

No end of infusion pre-alarm and alarm The installed syringe doesn't correspond with the selected syringe. Replace or confirm the right syringe brand. Recalibrate the position sensor Cal 3 with maintenance software. Flow rate or displacement control drift. The installed syringe doesn't correspond with the selected syringe. The position sensor calibration values have drifted. Check the position sensor calibration values and recalibrate it if necessary.

Change the position sensor. Occlusion alarm after the device has been turned on. Wrong calibration of the force sensor. Force sensor is out of order. Flexible circuit cut. Occlusion alarm during the infusion. The pressure limit selected is too low. Disengagement alarm after the device has been turned on or during the infusion. The disengagement micro-switch is defective. Carriage flexible circuit is cut. Unjustified alarm of plunger head position. Recalibrate and check the force sensor.

Replace the force sensor. Replace the flexible circuit. Select a higher pressure limit. Replace the micro-switch.

Replace the flat ribbon cable. Check the anti-siphon system Check the good condition of the pusher internal mechanism. Defective syringe holder potentiometer. Flat ribbon cable is defective. Check the syringe holder and replace the defective parts if necessary. Display defect: LED, screen. Check the good condition of the display board.

ISDN AND BROADBAND ISDN WILLIAM STALLINGS PDF

Injectomat Agilia®

.

AFFORDABLE AUTOMATION SABRIE SOLOMAN PDF

service manual

.

EBBINGHAUS BIOGRAFIA PDF

user's manual-injectoma agillia

.

CATALOGO CORREIAS DAYCO PDF

Injectomat Agilia Technical Manual Eng

.

Related Articles