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Description

The Accu-Chek Guide blood glucose monitoring system is designed to simplify diabetes management. It features a spill-resistant SmartPack® vial, a wide test strip dosing area, and a strip port light for easy testing anytime. The system includes wireless connectivity with the mySugr diabetes management app, which automatically logs results to your smartphone. The Accu-Chek Guide meter delivers advanced 10/10 accuracy for reliable results.

Specifications

• Display: LCD with backlit display

• Dimensions: 77.1 mm (length) x 48.6 mm (width) x 15.3 mm (height)

• Weight: Approximately 43 g (with batteries)

• Memory Capacity: Stores up to 720 tests, including 7, 14, 30, and 90-day averages

• Battery: Uses two CR2032 lithium coin cell batteries

• Connectivity: Bluetooth® enabled for wireless transfer to the mySugr app; USB port for PC connectivity

• Measurement Range: 0.6-33.3 mmol/L

• Measurement Time: Less than 4 seconds

• Sample Size: 0.6 μL

• Operating Temperature: 4°C to 45°C

• Storage Temperature: -25°C to +70°C (meter only); 4°C to 30°C (meter with batteries and strips).

Usage

1. Prepare the Meter: Insert a test strip into the meter. The meter will turn on automatically.

2. Lance Your Finger: Use the Accu-Chek Softclix lancing device to obtain a small drop of blood.

3. Apply Blood to the Test Strip: Place the drop of blood on the wide yellow edge of the test strip.

4. Read the Result: The meter will display your blood glucose level within seconds.

5. Log Results: Results are automatically logged to the mySugr app via Bluetooth for easy tracking and analysis.

Caution

• Choking Hazard: Keep small parts away from children under the age of 3 years.

• Use Only as Directed: The system is intended for single-patient use and should not be shared.

• Check Expiry Dates: Ensure test strips are not expired to avoid inaccurate results.

• Storage Conditions: Store the meter and test strips as per the specified temperature ranges to maintain accuracy.

• Medical Device Correction: Be aware of any urgent medical device corrections or recalls related to the product.