dretec Pulse Oximeter OX-202 Green

Coolbe: This product is a medical device which must be used only as intended and in accordance with the instructions for use. This device is not a substitute for professional medical advice, diagnosis, or treatment. Consult a qualified healthcare professional before use if in doubt. The seller/distributor is not liable for any damages arising from misuse, unauthorized modification, or use beyond stated indications.

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Please be sure to read the instruction manual.

Generic Name Pulse Oximeter

Product Name Pulse Oximeter OX-202

Warning - Do not use inside or in conjunction with a hyperbaric oxygen device. (This may cause malfunction, damage, or failure.) - Do not use in the presence of flammable substances (anesthetic gas, high-concentration oxygen, gasoline, etc.) or flammable vapors. (This may cause a fire.)

Contraindications/Prohibitions Intended Use (Patients) - This device is intended for patients weighing 15 kg or more and with a finger thickness of 8 mm or more. Do not use on infants or young children under these ages. - If you use a pacemaker, consult your doctor before using a pulse oximeter. Concomitant Medical Devices - Do not use in areas controlled by radiation equipment or MRI (magnetic resonance imaging) equipment. (This may cause malfunction, damage, or failure.) How to Use - Do not wear the device for long periods of time or continuously. - Do not wear on injured fingers.

Product Specifications [Measurement Range] SpO2: 70% - 99% Pulse: 30 bpm - 250 bpm PI: 0.3% - 20.0% [Measurement Accuracy] SpO2: 70% - 99%: ±2% (no specification for values below 70%) Pulse: 30 bpm - 100 bpm: ±2 bpm, 100 bpm - 250 bpm: ±2% PI: 0.3% - 1.0%: ±0.2%, 1.1% - 20.0%: ±2.0%

Precautions for Use (1) Conditions of Use and Basic Precautions ① Read the instruction manual before use. ② Do not use for purposes other than measuring blood oxygen saturation, pulse rate, and perfusion index. ③ Do not repair or modify. ④ Do not use on anything other than your fingers. ⑤ Keep the finger clean. (2) Precautions During Use ① If a malfunction is detected in the device, discontinue use immediately. ② If you notice any abnormalities in your body or the device, discontinue use immediately. ③ Do not use simultaneously with medical devices such as electrosurgical devices. ④ Do not move your finger or body during measurement. ⑤ Measurement may not be accurate in the following cases: ・When there is a high amount of abnormal hemoglobin (such as carboxyhemoglobin) ・When pigments (such as methylene blue) are present in the blood ・When blood circulation at the measurement site is insufficient ・When the device is worn on the same arm as the blood pressure monitor ・When ambient light, such as lighting, fluorescent light, or direct sunlight, is too strong ・When you have nail polish or hand cream on your nails ・When the device is not worn correctly on your finger ・When you are moving around violently ⑥ Do not pull on the device by the strap. (3) Precautions After Use ① After use, wipe the finger holder with a cloth soaked in rubbing alcohol. ② To clean, wipe with a soft cloth dampened with water or mild detergent, then dry with a dry cloth.

Maintenance and Inspection Information (1) If you notice any malfunctions or abnormalities with this product, contact the appropriate contact information. (2) When using this product after a period of inactivity, verify that it is operating normally and safely before use.

Manufacturer and Distributor Name Manufacturer: Doretec Co., Ltd. Manufacturer: Shenzhen Yimi Life Technology Co., Ltd. Country: People's Republic of China Contact Information Doretec Co., Ltd. Customer Service Center 2-3-9 Ryutsu Danchi, Koshigaya City, Saitama Prefecture 343-0824 Tel: 0120-875-019 (Monday-Friday 9:00-12:00, 13:00-17:00, excluding public holidays and company-designated holidays)

Purpose of Use or Effects/Efficacy Measure and display transcutaneous arterial blood oxygen saturation. Medical Device Classification: Special Maintenance Management Medical Device/Special Management Medical Device Medical Device Certification Number: 304AKBZX00072000