FreeStyle Libre Flash Accuracy Study

Exclusion Criteria

• •Subject has known allergy to medical grade adhesive or isopropyl alcohol used to disinfect skin.
• •Subject is pregnant, attempting to conceive or not willing and able to practice birth control during the study duration (applicable to female subjects only).
• •Subject has extensive skin changes/diseases at the proposed application sites that could interfere with device placement or the accuracy of interstitial glucose measurements. Such conditions include, but are not limited to extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, dermatitis herpetiformis, skin lesions, redness, infection or edema.
• •Subject is currently participating in another clinical trial.
• •Subject has donated blood within 112 days (3.7 months) prior to the beginning of the study activities.
• •Subject is anemic as determined by the Investigator.
• •Subject has concomitant medical condition which, in the opinion of the investigator, could interfere with the study or present a risk to the safety or welfare of the subject or study staff. Such conditions include but are not limited to History of HIV, Hepatitis B or C.
• •Subject has X-ray, MRI or CT appointment scheduled during the period of study participation, and the appointment cannot be rescheduled for a time before study participation starts or after study participation ends.
• •Subject is unsuitable for participation due to any other cause as determined by the Investigator.