Acheron Instruments announce its successful coordination with GS1 for a Unique Device Identification (UDI) system for surgical instruments.
To meet the global regulatory standards, Acheron Instruments has integrated with GS1 to get UDI, a vital step towards fulfilling the international requirements defined by the European Union Medical Device Regulation (EUMDR) and United States Food and Drug Administration (USFDA). We have directly purchased this software from GS1 to provide our customers with efficient compliance with our latest implementations.
The Unique Device Identification (UDI) system assigns medical instruments a unique identity, ensuring lifelong trackability which improves the supply chain. To identify them, the tools or packaging include a barcode or QR code. This unique code presents information about the device identification, production features, and expiry date, making it easier to manage the instruments efficiently.
Our company has obtained this software from GS1, a UDI issuing agency that provides a global framework to identify, capture and share medical device product information, thereby enabling a consistent worldwide implementation of UDI. It helps maintain the global marketplace standards.
However, Acheron Instruments, one of the leading manufacturers of surgical instruments in Pakistan, aims to utilize this software to enhance product quality, safety, and traceability. This innovation also focuses on addressing global healthcare needs. By executing this system, we ensure meeting global regulatory standards, enabling an extra layer of confidence in our products. With the help of UDI, we are dedicated to meeting the benchmark of global standardization given by the EU MDR and US FDA.
