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What AI should be used for software version under the EU MDR and IVDR?
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Does any change within the medical devices certification process require a new GTIN?
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What are the obligations of economic operators and health institutions in relation to UDI under EU MDR and IVDR?
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How do I create a Basic UDI-DI with GS1 standards?
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Where can I find information about EUDAMED?
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How should a UDI appear on the label or package of a device?
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Which AI should I use to encode your internal part number or SKU in the barcode for internal tracking?
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Is the deadline for UDI compliance extended if the product needs direct marking?
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Is it necessary to use the same GS1 Company Prefix (GCP) for the Basic UDI-DI (GMN) and its related UDI-DIs (GTINs)?
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Our company licensed a GS1 Company Prefix originally with a capacity of 100 GTINs. We now have more than 100 products, how do I get capacity for more GTINs?