User's Manual
Table Of Contents
- Table of contents
- List of figures
- CHAPTER 1 Description
- CHAPTER 2 Indications and contraindications
- CHAPTER 3 Personal Pump Communicator (PPC)
- CHAPTER 4 Pump implantation
- Preprogramming and pre-testing the Pump
- CHAPTER 5 Pump refill procedure
- CHAPTER 6 Explanting the Pump System
- CHAPTER 7 Warnings and precautions
- CHAPTER 8 Adverse reactions
- CHAPTER 9 System alarms and messages
- Pump alarms
- Alarm feedback
- Pump low battery
- Depleted pump battery
- System error
- Pump self test fail
- PPC low battery
- PPC alarms
- Low reservoir
- Empty reservoir
- Telemetry communication error
- Initialize alarm
- PPC not initialized
- Battery replacement
- Initialize to factory defaults
- Pump stopped
- Pump suspended
- Auto off
- Hourly maximum exceeded
- Pump alarm table
- Pump alarms
- CHAPTER 10 Troubleshooting Pump System under-delivery
- CHAPTER 11 Technical specifications
- APPENDIX A Label information symbol dictionary
- APPENDIX B Implant worksheet
- APPENDIX C Refill form
- APPENDIX D Precautions and general procedures
- APPENDIX E Pump rinse procedure
- APPENDIX F Side Port Catheter flush procedure
- Supplies and solutions
- Preparing for the procedure
- Flushing the Side Port Catheter
- Program minimal basal rate
- Remove insulin and fill with rinse buffer
- Equilibrate and pull rinse buffer through system
- Flush side port catheter
- Remove rinse buffer and fill with insulin
- Equilibrate and pull insulin through system
- Remove guide needles and record refill amount
- Program new basal rate
- Remove rinse buffer from catheter
- APPENDIX G Stroke volume measurement
Warnings and precautions
84
Physicians should instruct patients to avoid any sharp blows or pressure directly
at the Pump location. A direct hit by an object such as a baseball may damage the
Pump and/or injure the Pump pocket. Extreme pressure on the Pump may cause
the sutures and the tissue pocket to be damaged. As a result, the Pump may move
from its pocket and possibly dislodge from the Catheter.
If the Pump has been damaged by such a blow, the patient should be instructed to
contact their physician. Physicians may order a pressure bandage or a reduction
in the patient’s physical activity until the pump pocket reheals completely.
• Exposure to Extreme Body Temperatures
Exposure to elevated body temperatures in excess of 104°F (40°C) will
compromise the negative pressure reservoir safety feature of the Medtronic
MiniMed 2007D Implantable Pump. Glucose levels should be monitored closely
if this occurs.
Sterilization
The Pump, Catheter and the refill kit are sterilized with ethylene oxide (EtO).
The Pump System is NOT Reusable.
If the sterile package has been opened, damaged or tampered with DO NOT USE
the packaged device.
NOTE: Do Not Re-Sterilize the Implantable Insulin Pump
NOTE: Do Not Re-Sterilize the Side Port Catheter
NOTE: Do Not Re-Sterilize Components of the Refill Kit.
The Pipette (MMT-4104), may be resterilized using autoclave, EtO or according
to hospital procedures.
The Template (MMT-4106) may be resterilized using steam autoclave or EtO per
hospital procedure. This template is made from polycarbonate plastic and will
have a limited life in steam autoclave cycle. The template will not withstand dry
heat autoclave cycles.