After clinical use, devices are carefully packaged according to NEScientific Handling Instructions to minimize potential damage and maximize reprocessing success. Customers then schedule a FedEx® pickup using pre-paid labels, ensuring safe and efficient delivery to NEScientific.
Upon arrival at NEScientific, devices undergo an initial inspection to identify any issues or irreparable damage that could prevent reprocessing. While NEScientific continuously enhances its reprocessing capabilities, strict quality control guidelines ensure only acceptable devices move forward in the process.
Each device undergoes a rigorous decontamination and cleaning process tailored to its specific type. Throughout the production cycle, devices are meticulously inspected at multiple stages to ensure quality and compliance.
NEScientific’s proprietary technology enables highly effective cleaning methods, preparing devices for safe clinical reuse. Each device is tracked with a detailed history record to ensure every step of the process is completed with precision.
Devices undergo individual inspection and functionality testing. Once all requirements are met, each device is carefully pouched, labeled, and prepared for sterilization.
After completing the reprocessing cycle, devices are sterilized using 100% ETO. Post-sterilization testing ensures all requirements are met, followed by a final inspection to confirm readiness for sale.
The NEScientific Quality team verifies that each device meets all required internal specifications. Once approved, devices are added to inventory and made available for purchase by customers.
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