Search results with tag "Minimed"
Guardian Sensor (3) - MiniMed Insulin Pump Therapy
www.medtronicdiabetes.comMiniMed® 670G system to continuously monitor glucose levels in persons with diabetes. It is intended to be used for detecting trends and tracking patterns in persons aged fourteen years and older, and to be used by the MiniMed 670G system to automatically adjust basal insulin levels. It is indicated for use
（検8）05資料4 門脇構成員 随時血糖値の判定基準について …
www.mhlw.go.jp測定方法：Minimed Gold (Medtronic, Inc)を用いた持続血糖測定 （Continuous Glucose Monitoring：CGM） (資料11: 田嶼尚子ら. Daily Glucose Profiles in Japanese People with Normal Glucose Tolerance as Assessed by Continuous Glucose Monitoring. DIABETES TECHNOLOGY & THERAPEUTICS 11:457, 2009 )
Formulary Exception/Prior Authorization Request Form
www.caremark.coma. Test strips: Does the patient have an insulin pump? If yes, please provide make and model (e.g., OmniPod, MiniMed 530G)_____ Does the patient have an insulin pump that is incompatible with Accu-Chek or OneTouch product? Yes or No b. CGM: Is there a clinical reason why the patient cannot switch to Dexcom?
MINIMED MOBILE APP - Medtronic Diabetes
www.medtronicdiabetes.comThe MiniMed™ Mobile app is intended to provide a secondary display for a compatible MiniMed™ insulin pump system on a suitable consumer electronic device for passive monitoring and to sync data to CareLink™. The MiniMed™ Mobile app is not intended to replace the real-time display of continuous glucose monitoring
MiniMed 630G Transfer Settings Guide - Medtronic Diabetes
www.medtronicdiabetes.comMiniMed® 630G Replacement Pump STEP 1: Before you send your original pump back, copy your current settings onto the Insulin Pump Settings Form. If for any reason you cannot copy the settings, please contact your healthcare professional or reference your CareLink® Personal reports. STEP 2: Insert a AA battery into your new pump.
MiniMed 670G System - Medtronic
www.medtronic.comMedtronic is the first company to initiate and complete a U.S. pivotal trial of hybrid closed loop technology. The data from this study was included in its PMA submission to the FDA in June 2016 – the first and only company to file for commercial approval.