My Medic

My Medic specializes in manufacturing aneroid manual sphygmomanometers, which are blood pressure measurement devices. These devices use a manual pump and dial gauge to measure systolic and diastolic blood pressure without mercury, making them suitable for both clinical and home use.

My Medic is based in the United States. The company’s devices are designed to meet US regulatory standards for blood pressure measurement instruments.

My Medic’s sphygmomanometers fall under Class II medical device classification by the FDA. This classification applies to devices that generally present a potential for moderate risk and require special controls to ensure safety and effectiveness.

Yes, My Medic’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices to ensure traceability and compliance with regulatory requirements.