Smiths Medical International Ltd.
3200 Service Manual
Issue 5 (August 2004)
Page x
Warnings and cautions
AC input power connecting socket/cable
The AC input power socket that connects to the rear of the pump has three connections (live, neutral and earth)
provided by a 3-way power cable. As the casing is doubly insulated, the AC input connector situated on the pump
only utilises two connections (live and neutral), there is no third earth pin. This method of AC input enables similar AC
input sockets (if required) to that supplied by Smiths Medical to be used.
Introduction
This Technical Service Manual together with the Instruction Manual, contains all the information that is needed in order
to maintain, repair and operate the Graseby 3200 pump. The contents of this Manual are intended to be read and used
by suitably qualified personnel.
Warnings and cautions
Warnings tell you about dangerous conditions that could lead to death or serious injury to the user or patient that can
occur if you do not obey all of the instructions in this manual.
WARNINGS
1. WARNING: To avoid over- or under- infusion, always verify that the brand and size of the loaded syringe are the
same as the brand and size displayed on the screen before starting an infusion. Failure to do so may result in an
inaccurate delivery of medication, resulting in patient injury or death.
2. WARNING: To avoid incorrect or inappropriate configuration of the pump, the Configuration menu must only be
selected by qualified persons or authorised personnel. Incorrect pump configuration could lead to inappropriate
infusion resulting in patient injury or death.
3. WARNING: This equipment is not suitable for use in the presence of flammable anaesthetics, oxygen-enriched
or explosive atmospheres. The use of the device in such atmospheres may lead to explosion or fire.
4. WARNING: To avoid possible malfunction of the pump, do
not expose the pump to X- rays, gamma rays or
ionizing radiation, or to the RF interference or strong electric/magnetic fields emitted (for example) by diathermy
equipment or mobile telephones. If the pump is used in the presence of, or in combination with Magnetic
Resonance Imaging (MRI) machines it must be protected from the magnetic field emitted by such equipment.
Malfunction of the pump can cause incorrect infusion or loss of infusion resulting in patient injury or death.
5. WARNING: Operation of the pump outside the temperature limits defined in the specification may result in
erroneous operation. Ensure that the temperature is within the specified limits. Failure to do so may result in
patient injury or user injury.
6. WARNING: In order to ensure that the intended infusion is performed, data must be entered correctly. Likewise
before confirming any displayed data the user should ensure that it is correct. Failure to do so may result in
compromised function of the product, patient injury or user injury.
7. WARNING: Failure to respond promptly to an alarm may result in patient injury or death.
8. WARNING: Failure to follow the
Service Manual’s maintenance schedule recommendations may result in
compromised function of the product and lead to patient injury or death.
9. WARNING: It is essential that clinical staff remain within visual and audible range of the pump so that critical
alarms can be seen or heard and responded to.
10. WARNING: The user should ensure that the performance offered by the pump is fit for the intended purpose.
Failure to do so may result in compromised function of the product, patient injury or user injury.
11. WARNING: When the pump is carrying out an infusion, to ensure that electrical safety is maintained only items
of equipment that conform to EN60950 are to be connected to the RS232 connector situated at the base of the
pump, otherwise patient safety may be compromised.
12. WARNING: Correct management of battery charging is essential to ensure that the pump can operate on
batteries for the time specified. Failure to do so may lead to impaired functioning of the pump, resulting in
patient injury or death.
13. WARNING: Do
not use a faulty pump. If the pump develops a fault then an alarm will sound; the display will
indicate a FAULT condition and the pump will fail to infuse. Incorrect performance of the pump can cause
complications resulting in patient injury or death.
If the pump develops a fault then it must be referred to a suitably qualified engineer or returned to Graseby
Medical in order to have the fault rectified.
14. WARNING: Failure to use the mains lead clamp means that the pump may be accidentally or erroneously
disconnected from the mains. Although there is battery backup in case this happens, the battery may not be
sufficiently charged. Consequently there is a risk of the pump not functioning, which could lead to patient injury
or death.
15. WARNING: If an occlusion alarm occurs, immediately clamp the line to eliminate the possibility of a bolus being
delivered to the patient. Then inspect the fluid pathway for kinks, clogged catheter, etc. in order to remove the
occlusion prior to restarting the infusion. An unintentional bolus of medication can result in patient injury or
death.
Summary of Contents for Graseby 3200
Page 15: ...CHAPTER 1 INTRODUCTION FEATURES and SPECIFICATION 3200 In line Pressure Syringe Pump ...
Page 22: ...CHAPTER 2 CONFIGURATION DIAGNOSTICS and OCCLUSION THRUST 3200 In line Pressure Syringe Pump ...
Page 37: ...CHAPTER 3 FUNCTIONAL DESCRIPTIONS 3200 In line Pressure Syringe Pump ...
Page 43: ...CHAPTER 4 CIRCUIT DESCRIPTIONS 3200 In line Pressure Syringe Pump ...
Page 83: ...CHAPTER 6 FUNCTIONAL TESTS and MANUFACTURNG SETTINGS 3200 In line Pressure Syringe Pump ...
Page 91: ...CHAPTER 7 ILLUSTRATED PARTS LIST 3200 In line Pressure Syringe Pump ...
Page 105: ...CHAPTER 8 BRAUN PERFUSOR CONVERSION 3200 In line Pressure Syringe Pump ...
Page 108: ...CHAPTER 9 DC INPUT VERSION of 3200 3200 In line Pressure Syringe Pump ...
Page 111: ...APPENDIX FITTING a MODIFIED SIZE SENSOR FLAG 3200 In line Pressure Syringe Pump ...
