The MiniMed ™ 630G systemLow glucose suspendSUGAR.IQ ™ SMART ASSISTANTOnly Guardian ™ Connect CGM powered by Guardian ™ Sensor 3 works with the Sugar.IQ ™ personal diabetes assistant, which supercharges your understanding of daily glucose patterns and the factors affecting them. ∆ EXCLUSIVE CARELINK ™ SOFTWAREA web-based program that collects information directly from your Medtronic diabetes management system.
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What's new in this version: Data Guardian 5.0.1 - Change log not available for this version Data Guardian 5.0 - Minor bug fixes. Latest Data news, comment and analysis from the Guardian, the world's leading liberal voice.
It allows you to generate reports that can be used during your doctor’s visits and to monitor your own progress. Refers to Auto Mode. Some user interaction required.
Individual results may vary. Data on file.
The Guardian™ Connect system is indicated for ages 14 to 75. The MiniMed™ 670G system is indicated for ages 7 to 75. The MiniMed™ 630G system is indicated for 14 years of age and older.‡ Arm indication approved for ages 14-75.† dQ&A Diabetes Educator Perspectives Survey, Q3 2015. 428 total respondents. When compared with other software that downloads both insulin pump and continuous glucose monitoring data, CareLink is the #1 preferred software.∆ The system is intended to complement, not replace, information obtained from standard blood glucose monitoring devices.
All therapy adjustments should be based on measurements obtained from standard blood glucose monitoring devices and not on values provided by the system.†† At the time of manufacture and when the reservoir and tubing are properly inserted, the pump is waterproof. It is protected against the effects of being underwater to a depth of up to 12 feet (3.6 meters) for up to 24 hours.1 MiniMed ™ 670G System SSED. Accessed July 31, 2018. Arm insertion, 3-4 calibrations per day.Important Safety Information: Guardian ™ Connect CGM SystemThe Guardian ™ Connect system requires a prescription and is indicated for continuous or periodic monitoring of glucose levels in the interstitial fluid under the skin, in patients (14 to 75 years of age) with diabetes mellitus.
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The system is intended to complement, not replace, information obtained from standard blood glucose monitoring devices, and is not recommended for people who are unwilling or unable to perform a minimum of two meter blood glucose tests per day, or for people who are unable or unwilling to maintain contact with their healthcare professional. The system requires a functioning mobile electronic device with correct settings. If the mobile device is not set up or used correctly, you may not receive sensor glucose information or alerts.
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January 2023
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