Import Dk-8000d Portable Patient Monitor — Buy in Bulk from Supplier in China

The DK-8000D portable patient monitor is a compact medical device designed for real-time monitoring of vital signs in clinical and emergency settings. It features a 15-inch color TFT display capable of showing up to 14 simultaneous waveforms, including ECG, RESP, and SpO2. The device operates on rechargeable battery and AC power, with a one-level menu interface for rapid access during critical situations.

The monitor uses pulse oximetry technology with a SpO2 accuracy of ±2% within the 70 - 100% range, consistent with ISO 80601-2-61 standards. ECG measurements are derived from a 3-lead configuration with noise filtering and arrhythmia detection. The system does not include invasive blood pressure or end-tidal CO2 monitoring. The display resolution is 1024x768 pixels, optimized for visibility under low-light and bright ambient conditions.

This monitor is primarily used in hospital emergency departments, ambulances, and outpatient clinics where mobility is essential. Buyers include regional healthcare providers in Africa, Southeast Asia, and Latin America who require cost-effective, durable equipment. Units are shipped in padded hard-shell cases with spare sensors and a charger. Trade terms are typically FOB Shenzhen, with lead times of 20 to 30 days after payment confirmation. Custom firmware updates or language packs are available upon request.

Shenzhen Adecon Technology Co., Ltd. is a manufacturer located in Shenzhen, Guangdong Province, with its registered facility at 2/F, Plant No.1, Shangrong Industrial Park. The company is classified as an imported supplier with harbor trust tier, indicating verified export history. There is no public data on years of operation, staff size, or quality certifications such as ISO 13485 or CE marking. The listing does not confirm clinical testing or regulatory compliance beyond general claims.

The supplier has no documented response rate or average response time, suggesting limited buyer interaction. No product manuals, test reports, or firmware version history are referenced. Buyers should request a copy of the CE Declaration of Conformity, IEC 60601-1 compliance statement, and a list of approved accessories. Without these, the device may not meet import or clinical use requirements in many jurisdictions.