ASTM F2847 Standard Practice for Reporting and Evaluation of Residue in Disposable Implants

EUROLAB laboratory provides testing and compliance services within the scope of ASTM F2847 standard. The purpose of this application is to explain how to report the cleanliness of manufactured disposable implants. This application suggests how to approach the identification of critical compounds and proposes different analytical methods.

The app does not address items specific to implant features or design. Specifically, by design it does not address substances released during implant resorption, implant coatings, or leaks.

This practice does not address the cleaning of reprocessed, re-cleaned implants after they have been unpacked for reuse in the hospital or by the manufacturer.

This application recommends suitable test methods for the general properties of the residues and the residue requirements of the implants. This application can also be used to characterize semi-finished components for implants.

This standard does not purport to address all, if any, safety concerns associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and to determine the applicability of regulatory restrictions prior to use.

EUROLAB assists manufacturers with ASTM F2847 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.