INTERNATIONAL FILTER PRODUCTS, INC.

International Filter Products, Inc. specializes in intravenous administration devices. Their primary products include intravenous administration bags or bottles and basic noninvasive intravenous administration sets. These devices are used to deliver fluids like medications, nutrients, or hydration solutions directly into a patient’s bloodstream in clinical settings.

International Filter Products, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, as it operates within the FDA’s jurisdiction.

The devices produced by International Filter Products, Inc.—such as intravenous administration bags and noninvasive sets—are classified as Class II under FDA regulations. This classification indicates a moderate level of risk, requiring special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

Yes, the devices manufactured by International Filter Products, Inc. are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, improving transparency and traceability in healthcare settings.