CPRP LLC

CPRP LLC specializes in reusable freestanding patient positioners. These devices are designed to help position patients securely and efficiently during medical procedures or imaging, improving both patient stability and ease of use for healthcare providers. The focus is on clinical settings where precise positioning is critical.

CPRP LLC is based in the United States. The company’s location means its devices are subject to U.S. regulatory requirements, including compliance with FDA guidelines. Since the devices fall under FDA Class I classification, they are generally considered lower risk but still require adherence to manufacturing and labeling standards.

Yes, CPRP LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability and transparency in the medical device supply chain. Listing in the UDI database allows healthcare providers, regulators, and other stakeholders to quickly identify and verify the device’s details, such as its manufacturer and classification, which is particularly useful for compliance and recall purposes.

CPRP LLC’s devices are classified as FDA Class I medical devices. This classification is based on their intended use—freestanding patient positioners—which are considered low-risk due to minimal potential harm if they malfunction. Class I devices typically require general controls (like proper labeling and manufacturing practices) but do not always need pre-market approval, though compliance with FDA regulations remains essential.