//Medical Devices

Strictly following regulations and best pratices

R&B Medical Devices

For the past years a unique standard for the identification medical devices has been discussed worldwide. The U.S. Food and Drug Administration (FDA) was the first national agency to regulate the topic and selected the GS1 standard to perform the unique identification of the health products by labeling products’ packages or in some cases the product itself.

Using its know-how in traceability and seeking to support this important segment within the healthcare industry, R&B developed a traceability system, R&B Medical Devices, specific for medical devices’ manufacturers and vendors, totally adequate to the GS1 UDI (unique device identifier) standard.

The R&B Medical Device system enables compliance with legal provisions; better control across supply chain, which is becoming increasingly relevant given the great flow of products around the world; provides promptness and accuracy regarding recall processes, requirements needed in adverse events impacting patients’ health; in addition to integration to clinical information systems and electronic records.

EG Mont, a company with over 15 years of experience in the health product sector, is R&B exclusive commercial partner in distributing this system.

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