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CLEMENTS

CLEMENTS

CLEMENTS

CLEMENTS 

 

 

 

30

 

Warranty

 

ICU  Medical  Australia  Pty  Limited  ("ICU  Medical  Australia")  warrants  that  this 
product  is  free  from  defects  in  workmanship  and  materials  for  a  period  of  24 
months  (3  months  for  batteries)  from  the  date  of  shipment  by  ICU  Medical 
Australia or its authorised agent to  the purchaser. Subject to the conditions of 
this warranty, if the product fails to operate for any reason within the warranty 
period  and  the product  is  returned  to  the place of  purchase at  the purchaser's 
expense, ICU Medical Australia will repair or replace the product free of charge. 

If a valid warranty claim is made within 30 days from the date of shipment, then 
ICU  Medical  Australia  will  also  reimburse  the  purchaser  for  reasonable  freight 
costs in returning the product to the place of purchase. 

Conditions of Warranty

 

1. 

The  product  must  be  returned  to  the  place  of  purchase  with  proof  of 
purchase. 

2. 

This warranty is only available to the original purchaser of the product. 

3. 

The  product  must  not  have  had  its  serial  number  removed,  defaced  or 
changed,  its  casing  opened,  its  power  supply  altered  or  have  been 
tampered with in any other way. 

4. 

This warranty does not cover : 

• 

inadequate or incorrect site preparation; 

• 

improper installation; 

• 

connection to the wrong voltage; 

• 

failure of the product due to misuse; 

• 

the use or  operation of  the product outside of  the physical,  electrical or 
environmental specifications of the product; 

• 

use in a manner or environment in which the product is not designed to 
be used; 

• 

improper adjustment, calibration or operation by the purchaser; 

• 

the  use  of  accessories  including  consumables,  hardware  or  software 
which  were  not  manufactured  or  approved  in  writing  by  ICU  Medical 
Australia; 

• 

any modifications of the product which were not authorised in writing by 
ICU Medical Australia; 

• 

any contamination or leakages caused or induced by the purchaser; and 

• 

inadequate or improper maintenance of the product. 

5. 

This warranty does not cover normal wear and tear. 

6. 

ICU  Medical  Australia  will  not  be  responsible  for  damage  or  loss  caused 
during shipping. 

Warranty 

Содержание SUC84602

Страница 1: ...HiFlo2 High Vacuum High Flow Mobile Suc on Pump SUC84602 220 240V 50 60Hz User Manual CLEMENTS Manual No SUC84602008 Issue 3...

Страница 2: ...operated by authorised personnel in accordance with the instructions as described in this manual Operated in this way the HiFlo2 High Suction Pump will provide the standard of service specified Due to...

Страница 3: ...autions 9 Important Safety Rules 10 Controls and Operation 13 Using FLOVAC Liners 15 Cleaning 16 Spare Parts 19 Troubleshooting 21 Wiring Diagram 22 Diagnostic Setup 23 Periodic Safety Check 25 Emissi...

Страница 4: ...and authorized personnel Contraindications Before using the HiFlo2 consult the instructions for use Failure to follow the instructions in this manual could cause harm Do not use the HiFlo2 for thorac...

Страница 5: ...r 2x 2 litre autoclavable reusable jar Optional 5 litre autoclavable reusable jar Optional 2 litre disposable liner jar Optional 3 litre disposable liner jar Overfill Protection Float valve mechanism...

Страница 6: ...posable antibacterial hydrophobic filter Stepped conical tubing connector Environmental Conditions Environmental conditions for operation transportation and storage are shown in the following table In...

Страница 7: ...Applied Part suction cannula Insulation Class II double insulation Hz Mains power frequency Alternating current On Off CE Mark in conformity with Regulation EU 2017 745 Manufacturer REF Model Referenc...

Страница 8: ...Symbols SN Serial Number Fragile Relative Humidity Range Keep Cool Keep out of direct sunlight Temperature Range Atmospheric Pressure Range Fuse C Tick Mark Dispose of electrical product according to...

Страница 9: ...of rating label matches that of the mains power 3 Avoid the use of power boards and extensions 4 Maintain clear access to the mains power outlet to facilitate disconnection 5 Place pump clear of patie...

Страница 10: ...hich may cause it to accidentally fall and lead to a malfunction and or breakage Should there be signs of damage to the plastic parts which may expose inner parts of the energised device do not connec...

Страница 11: ...ys contact technical assistance 8 Using the device in environmental conditions different than those indicated in this manual may harm seriously the safety and the technical characteristics of the same...

Страница 12: ...k of burns if you touch those parts In any case the temperatures do not exceed the limit of 105 C ref Interpretation Sheet IEC 60601 1 ISH May 2013 The manufacturer cannot be held liable for accidenta...

Страница 13: ...peripheral port to the VACUUM port of the collection jar 3 Connect the long silicone tubing to the collection jar PATIENT port 4 Connect supplied power cord to power socket at rear of pump Connect po...

Страница 14: ...er supply is required Suction Accessories The device and its accessories are biocompatible in accordance with EN 60601 1 Suction Cannulae Suction cannulae or suction probes for contact with the human...

Страница 15: ...5 If fluid reaches the maximum level the hydrophobic filter in the lid will operate to prevent further fluid flow When this happens switch off pump and replace liner Disposal 1 Switch off pump 2 Disco...

Страница 16: ...protocols for potentially biohazardous waste Clean Housing Wipe clean with a damp soapy cloth Do not immerse or allow liquid to enter the housing Do not use abrasive cleaning agents Accessories Before...

Страница 17: ...d by local protocols and compatible with silicone tubing Suction tubing may be autoclaved to a maximum of 121 C for 15 minutes At higher temper atures the suction tubing will discolour and lose shape...

Страница 18: ...suction tubing and replace if it is perished soft or discoloured Check the seal ring on the lid and replace if hard cracked or perished Check the fit of the lid in the collection jar canister Check t...

Страница 19: ...0112 Kit Liner Connect Nipple Pack 5 SUC84500123 Kit Disposable 3L Liner Pack 50 SUC84600120 Jar Trap 220mL for Mul purpose Rail SUC84600122 Jar Suc on Reusable 2L Complete SUC84600125 Jar Suc on Reus...

Страница 20: ...for 2L 3L FLOVAC Jar SUC84600113 Bracket Ring for Catheter Holder SUC84600114 Catheter Holder SUC84600160 Rail Stainless Steel Standard Medical 30 x 10 SUC84600201 Motor Pump for HiFlo2 200 240V 50 60...

Страница 21: ...ubing is in good condition and not old and cracked Check the type of handpiece in use as some handpieces require finger occlusion to assist suction Check trap jar Check bacteria hydrophobic shut off v...

Страница 22: ...CLEMENTS CLEMENTS CLEMENTS CLEMENTS 22 Wiring Diagram Wiring Diagram...

Страница 23: ...Disconnect all items from inlet and with pump switched off confirm that gauge reads zero A non zero reading indicates a faulty gauge Set vacuum control knob to maximum switch on pump and confirm that...

Страница 24: ...up Any difference indicates leaks in jar or connections 1 Occluded leak check Flow Check Max Vacuum Gauge Connect pump as shown in diagram Set vacuum control knob to maximum and switch on pump Connect...

Страница 25: ...dge and practical experience to perform these tests Inspect the equipment and accessories for mechanical and functional damage Inspect the safety relevant labels for legibility Verify that the device...

Страница 26: ...power supply network that supplies buildings used for domestic purposes EMC Information Tables per EN60601 1 2 2015 In accordance with EN 60601 1 2 2015 A1 2021 Medical electrical equipment Part 1 2 G...

Страница 27: ...put output lines The device doesn t change its state Mains power quality should be that of a typical commercial environment or hospital Surge EN 61000 4 5 1 kV differential mode The device doesn t cha...

Страница 28: ...d be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol Radiated Immunity EN 61000 4 3 3 V m 80 MHz to 2 7 GHz...

Страница 29: ...ansmitter W 150 kHz to 80 MHz d 3 5 V1 P 80 MHz to 800 MHz d 12 E1 P 800 MHz to 2 7 GHz d 23 E1 P 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 For transmitters with...

Страница 30: ...ble to the original purchaser of the product 3 The product must not have had its serial number removed defaced or changed its casing opened its power supply altered or have been tampered with in any o...

Страница 31: ...rms of the sale of the product or otherwise in connection with the product is limited to the amount paid by the purchaser to ICU Medical Australia for the product 10 Apart from any liability imposed b...

Страница 32: ......

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