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SILICONE PATIENT SPECIFIC IMPLANT DESIGN FORM1. SURGEON DETAILS Surgeon Name:Specialty:Email:Phone:2. PRODUCT DETAILS Region: ChestOptions: Suture tabsDurometry: Firm Face Arm Textured Medium Soft
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The qr-72-01-23 silicone implant design refers to a specific regulatory document or form used in the medical industry to provide detailed specifications and characteristics of silicone implants.
Manufacturers and distributors of silicone implants are required to file the qr-72-01-23 silicone implant design with the relevant regulatory authorities.
To fill out the qr-72-01-23 silicone implant design, one must follow the guidelines provided by the regulatory authority, including entering detailed information about the implant's dimensions, material composition, and intended use.
The purpose of the qr-72-01-23 silicone implant design is to ensure that silicone implants meet safety and efficacy standards before they are approved for use in patients.
The qr-72-01-23 silicone implant design must report information such as the product's design specifications, testing results, materials used, and any other relevant data that supports its safety and effectiveness.
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