J. W. HARRIS CO., INC.

J. W. Harris Co., Inc. specializes in medical air cylinder regulators and laboratory instrument gas monitors/regulators. These devices are engineered to ensure accurate control and monitoring of gas flow, which is critical in both clinical and laboratory environments to maintain safety and operational efficiency.

J. W. Harris Co., Inc. is headquartered in the United States. The company’s location ensures it operates within the regulatory framework of the FDA, which governs the design and distribution of its medical devices.

The devices produced by J. W. Harris Co., Inc., such as medical air cylinder regulators and laboratory gas monitors/regulators, fall under Class I classification according to FDA regulations. This classification typically applies to devices posing minimal risk to patients and users, often involving general controls like good manufacturing practices and labeling requirements.

Yes, the devices manufactured by J. W. Harris Co., Inc. are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability for regulatory and market surveillance purposes.