Omron Wrist Blood Pressure Monitor HEM-6180 Series HEM-6182

[Please refer to the instruction manual.] [General Name] Automatic Electronic Blood Pressure Monitor [Product Name] Omron Wrist Blood Pressure Monitor HEM-6180 Series

[Contraindications/Prohibitions] (1) Self-diagnosis of measurement results or treatment based on self-diagnosis [This may lead to a worsening of symptoms.] (2) Measurement on an injured or injured arm [This may lead to a worsening of symptoms.] (3) Measurement on an arm receiving intravenous infusion or blood transfusion [This may lead to a worsening of symptoms.] (4) Use near flammable or combustible gases [This may cause ignition, fire, or explosion.] (5) Use beyond the service life [This may result in inaccurate measurements.] (6) Use by an unspecified number of people in medical institutions or public places [This may cause accidents or problems.] ]

[Specifications] External dimensions: Approx. 93 (W) x 62 (H) x 20 (D) mm (excluding cuff) Weight: Approx. 86 g (excluding batteries) Operating environment conditions: +10 to +40℃ / 15 to 90% RH (non-condensing) / 800 to 1060 hPa Applicable wrist circumference: 13.5 to 21.5 cm

[Electrical ratings] Power supply: 2 x AAA alkaline batteries (DC 3V 3.0W) Electric shock protection: Internally powered equipment BF type applied part: Cuff IP protection rating: IP22

[Performance and safety standards] (1) Error in blood pressure measurement by clinical performance test: • Average error compared to auscultation method: ± 5 mmHg • Standard deviation: ± 8 mmHg (2) Error in cuff pressure display: ± 3 Within mmHg (3) Rapid Exhaustion: • Time required to rapidly exhaust from 260 mmHg to 15 mmHg: 10 seconds or less (4) Stability of Cuff Pressure Display: • Change in cuff pressure display value after 10,000 simulated measurements: 3 mmHg or less (5) Maximum Cuff Pressure: 299 mmHg

[Purpose of Use or Effect] To measure systolic and diastolic blood pressure non-invasively for home health management.

[Precautions for Use] 1. Individuals with severe circulatory disorders or blood diseases should use under the guidance of a physician. 2. Temporary internal bleeding may occur due to compression. 3. Do not use on infants or individuals unable to express their wishes. 4. Do not use for purposes other than blood pressure measurement. 5. Do not disassemble or modify the main unit or dedicated cuff. 6. Insert the battery with the correct + and - terminals. 7. Use the specified batteries. 8. Remove the batteries when not using the device for an extended period. [Manufacturer and Distributor Information] Manufacturer and Distributor: Omron Healthcare Co., Ltd. Phone: 0120-30-6606 (Omron Customer Service Center) Medical Device Classification: Specified Controlled Medical Device Medical Device Certification Number: 230AGBZX00002000