Product Info
Table Of Contents
- M998590A011DOC_A_FINAL_UserGuide_Part2
- Troubleshooting
- Maintenance
- Product specifications and safety information
- Product specifications
- Alarm and alert escalation
- Altitude range
- Audio frequency
- Backlight
- Basal delivery
- BG Target
- BG meter value
- Bolus delivery
- Bolus Wizard feature default settings
- Bolus Wizard feature specifications
- Carb ratios
- Delivery accuracy
- Easy Bolus feature
- Environmental conditions
- Essential performance
- Filling the infusion set and cannula
- Infusion pressure
- Insulin delivery default settings
- Bolus settings
- Basal settings
- Insulin sensitivity factor
- Low Reservoir reminder
- Max Bolus
- Normal bolus
- Occlusion detection
- Percent temp basal
- Program safety checks
- Pump dimensions
- Pump memory
- Pump weight
- Sensor default settings
- Wireless communication
- FCC notice
- IEC60601-1-2:4th Edition notice
- Guidance and manufacturer's declaration
- Icon glossary
- Product specifications
- 670G Performance Data and Technical Information
The Accu-Chek Guide Link Blood Glucose Monitoring System is intended for in
vitro diagnostic single-patient use by people with diabetes
The Accu-Chek Guide Link Blood Glucose Monitoring System is intended to be
used by a single person and should not be shared.
This system is not for use in diagnosing or screening for diabetes mellitus and not
for neonatal use.
Alternative site testing should be done only during steaty-state times (when
glucose is not changing rapidly).
The Accu-Chek Guide control solutions are for use with the Accu-Chek Guide Link
Blood Glucose Monitoring System to check that the meters and test strips are
working together properly and that the test is performing correctly.
The Accu-Chek Guide Link Blood Glucose Monitoring System is intended to be
used to wirelessly transmit glucose values to a compatible MiniMed pump with
Bluetooth wireless technology through the use of Bluetooth low energy
communication.
Contraindications
Pump therapy is not recommended for people whose vision or hearing does not
allow recognition of pump signals and alarms.
Do not use the serter on products other than the Guardian Sensor (3). Medtronic
cannot guarantee the safety or efficacy of this product if used with other products.
The reservoir is contraindicated for the infusion of blood or blood products.
Infusion sets are indicated for subcutaneous use only and not for intravenous (IV)
infusion or the infusion of blood or blood products.
Insulin pump therapy is not recommended for those who are unwilling to perform
at least four BG tests per day. As insulin pumps use rapid-acting insulin only, BG
testing is required to help identify rapid glycemic deterioration due to insulin
infusion occlusion, infusion site problems, insulin stability issues, user error, or a
combination of these.
SmartGuard Auto Mode cannot be used for people who require less than eight
units or more than 250 units of total daily insulin dose per day.
Pump therapy is not recommended for people who are unwilling or unable to
maintain contact with their healthcare professional.
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Before you begin
Before you begin 9