TREND POWER LIMITED

Trend Power Limited specializes in two primary device categories: infrared patient thermometers for measuring skin temperature and pulse oximeters, which monitor oxygen saturation levels in the blood. These devices are designed for both clinical and home use, such as the MOVE 78 Cold & Flu Kit, which combines these functionalities for non-invasive patient monitoring.

Trend Power Limited is based in the United States. This location aligns with FDA regulatory oversight, meaning its devices are subject to U.S. medical device classification and compliance requirements. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, reflecting their regulatory registration in the U.S. market.

Trend Power Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices under FDA jurisdiction, ensuring traceability and compliance with U.S. regulations. Listing in the UDI database is required for Class II devices, which includes Trend Power’s infrared thermometers and pulse oximeters.

Trend Power Limited’s devices are classified as Class II medical devices under FDA regulations. This classification applies to products that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness. Examples include infrared skin thermometers and pulse oximeters, which require validation of performance and labeling requirements to mitigate risks like inaccurate readings.