800 Luxurious Type B-ultrasonic Therapeutic

The 800 Luxurious Type B-ultrasonic Therapeutic device is a clinical-grade system designed for physiotherapy and pain management, equipped with a 3.5 MHz main probe featuring 80 array elements. This configuration enables high-resolution imaging and therapeutic ultrasound delivery, with a maximum depth capability of 200 mm for deep tissue examination and treatment. The device achieves transverse resolution of 2 mm and vertical resolution of 1 mm, ensuring precise diagnostics and targeted interventions.

Built with a user-friendly interface, the system is lightweight and portable, allowing for easy transport between clinical settings such as hospitals, rehabilitation centres, and private practices. The probe’s 80-element array is typical for mid-range therapeutic ultrasound devices, which often operate in the 1-5 MHz frequency range to balance penetration depth with image clarity. Standard devices in this category may include adjustable power outputs, typically ranging from 0.5 to 3 W/cm², to accommodate various treatment protocols.

This model is suitable for medical professionals seeking a versatile tool for pain relief, muscle rehabilitation, and soft tissue therapy. Buyers should confirm the device’s compatibility with their clinical workflows, including power requirements and software language options. The supplier, Shanghai Wiscon Medical Electronic Company, operates from Jiading Area, Shanghai, but trade terms such as MOQ, packaging, and certifications must be verified directly, as these are not explicitly detailed in the listing.

Shanghai Wiscon Medical Electronic Company is located at No.39 Chengzhong Road in the Jiading Area of Shanghai, a region known for its concentration of medical device manufacturers and suppliers. The company specialises in therapeutic and diagnostic equipment, with this listing highlighting its focus on ultrasound technology for clinical applications. The imported supplier tier indicates a history of engagement with international buyers, though no specific export markets are provided.

The profile does not disclose response rates, certifications, or production capacity, meaning buyers must directly confirm compliance with health and safety standards such as CE or FDA. The harbor trust tier suggests a baseline level of reliability, but additional verification - such as factory audits or third-party certifications - should be pursued for high-value medical equipment. No client references or case studies are available in the listed data.