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Inventory Control Form Titanium Dual-Opening USS Patient Information: SYNTHS (USA) To Order: (800) 523-0322 SYNTHS (Canada) Ltd. To Order: (800) 668-1119 Date: Hospital: Surgeon: Procedure: Dual-Opening
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What is synformsis 2 4mm cannulated?
Synformsis 2 4mm cannulated refers to a specific medical device used in surgical procedures. It is a cannulated device with a diameter of 4mm that is designed for synformsis, a surgical technique used to stabilize fractured bones in the body.
Who is required to file synformsis 2 4mm cannulated?
The filing of synformsis 2 4mm cannulated is not a requirement for individuals but rather for medical professionals and institutions that use or purchase the device for surgical procedures. These professionals and institutions are required to document the usage and purchase of such medical devices for regulatory and accounting purposes.
How to fill out synformsis 2 4mm cannulated?
Filling out synformsis 2 4mm cannulated does not pertain to a form or documentation process. It is a medical device used in surgical procedures and does not require any specific forms to be filled out. However, medical professionals using the device need to accurately record the usage and any relevant patient information in patient records or surgical reports.
What is the purpose of synformsis 2 4mm cannulated?
The purpose of synformsis 2 4mm cannulated is to provide stability and support in surgical procedures involving fractured bones. It is specifically designed to stabilize bone fragments and facilitate the healing process. The cannulated design allows for the insertion of additional screws or pins to further secure the fractured bone fragments.
What information must be reported on synformsis 2 4mm cannulated?
There is no specific reporting requirement for synformsis 2 4mm cannulated itself. However, medical professionals and institutions using the device should report relevant information such as patient identification, surgical procedure details, any complications or adverse events, and the usage of the device in medical records and reports as required by medical regulations and best practices.
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