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Bidder/Proposer/Statement of Qualifications Submitter (hereinafter collectively referred to as “Consultant “) must provide the information requested in the following sections/tables. 1. CONSULTANT
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Instructions for use of (IFU) are detailed documents that provide essential information on the proper use and handling of medical devices, products, or equipment.
Manufacturers of medical devices and products are required to file instructions for use for their respective products to ensure compliance with regulatory standards.
To fill out instructions for use, manufacturers should provide a clear description of the device, its intended purpose, detailed usage instructions, precautions, storage and handling information, and any other relevant information for safe and effective use.
The purpose of instructions for use is to inform users about how to correctly operate and maintain a product, ensuring safety and efficacy while minimizing risk during usage.
Instructions for use must report information that includes the device name, identification number, indications for use, contraindications, warnings, instructions for operation, maintenance guidelines, and contact information for the manufacturer.
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