Fetal monitor

The Fetal Monitor FD-2000K is a handheld Doppler device designed for clinical use in prenatal care, featuring a 2.0 MHz transducer probe for fetal heart rate detection between 85 and 210 beats per minute. It includes a 3.5-inch LCD display with backlight, rechargeable lithium-ion battery (1200 mAh), and continuous operation for up to 8 hours on a single charge. The device weighs 380 grams and measures 180 mm x 85 mm x 40 mm, making it suitable for use in clinics, maternity wards, and home visits.

The probe is compatible with standard gel-based coupling and operates within the FDA-recommended frequency range for obstetric Doppler devices. The device does not generate ultrasound output exceeding 94 mW/cm², aligning with IEC 60601-2-37 safety standards for diagnostic ultrasound. Typical industry variants include single-probe and dual-probe configurations; this model supports one probe type with fixed frequency. Standard packaging includes a protective carrying case, charging cable, and user manual in English and Chinese.

This device is primarily purchased by private obstetric clinics, rural health centers in developing regions, and midwifery practices seeking portable, low-cost fetal monitoring. Buyers typically order in batches of 5 to 50 units. Trade terms are offered as FOB Beijing or CIF destination port, with standard packaging in cartons of 10 units. Lead time is confirmed upon order, and warranty coverage is 12 months from shipment.

Beijing Greenland Science And Technology Development Co., Ltd is a registered supplier based in Haidian District, Beijing, with a physical address listed in official import records. The company is classified as an imported supplier with harbor-tier trust verification, indicating documented export history and compliance with basic customs documentation requirements. No public information confirms manufacturing capability, clinical testing, or R&D facilities; the listing does not state certifications, years in operation, or employee count.

The company appears to function as a trade intermediary for medical devices, sourcing products for export. Response rate and average response time are not available on the platform, suggesting limited buyer engagement or operational capacity. The product listing does not claim ownership of the FD-2000K design, nor does it reference ISO or CE certification as a manufacturer - only that the device is supplied under these standards. Buyers should verify direct compliance documentation before procurement.