Dretec OX-400 Pulse Oximeter, Gray

Coolbe: Dieses Produkt ist ein Medizinprodukt und darf ausschließlich bestimmungsgemäß und gemäß der beiliegenden Gebrauchsanweisung verwendet werden. Dieses Gerät ist kein Ersatz für professionellen ärztlichen Rat, Diagnose oder Behandlung. Wende dich bei Zweifeln vor der Anwendung an einen qualifizierten Arzt oder eine medizinische Fachkraft. Der Verkäufer/Vertriebspartner haftet nicht für Schäden, die aus unsachgemäßer Verwendung, unbefugter Modifikation oder einer Nutzung außerhalb der angegebenen Indikationen entstehen.

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[Please read the instruction manual carefully]

[Generic Name] Pulse Oximeter

[Product Name] Pulse Oximeter OX-400

[Warning] - Do not use inside or in conjunction with a hyperbaric oxygen device. (This may cause malfunction, damage, or breakdown.) - 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. Do not use on infants or young children under this age. - If you have 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 breakdown.) How to Use - Do not wear the device for extended periods or continuously. - Do not wear on injured fingers.

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

[Usage Precautions] (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 where the device is attached clean. (2) Precautions during Use ① If a malfunction is detected, discontinue use immediately. ② If you experience any abnormalities in your body or the device, discontinue use immediately. ③ Do not use simultaneously with medical devices such as electrosurgical units. 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 properly on your finger - When there is vigorous body movement ⑥ Do not pull 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 soaked in water or mild detergent, then wipe with a dry cloth.

[Maintenance and Inspection Matters] (1) If you notice any malfunctions or abnormalities with this product, please contact us. (2) When using this product after a period of inactivity, please confirm that it is operating normally and safely before use.

[Name of Manufacturer and Distributor] Manufacturer: Doretec Co., Ltd. Manufacturer: Shenzhen Yimi Life Technology Co., Ltd. Country of Manufacturer: 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 (Mon-Fri 9:00-12:00, 13:00-17:00, excluding public holidays and company-designated holidays)

[Purpose of Use] Measure and display transcutaneous arterial oxygen saturation. Medical Device Classification: Special Maintenance-Restricted Medical Device/Special Controlled Medical Device Medical Device Certification Number: 305AKBZX00055000