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”Who assigns the UDI-DI? | The manufacturer has to contact one of the issuing entities named by the European Commission. IFA GmbH is one of these issuing entities. “ more
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FAQ
”Where can I find the UN-Nummer for my product? | The UN-Nummer is stated on the Sicherheitsdatenblätter (safety data sheet) for products with hazardous substances.“ more
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FAQ
”For what purpose can I state the producer of Nahrungsergänzungsmittel, if it is not the supplier? | Stating the producer's address for Nahrungsergänzungsmittel is used for a transparent country of origin.“ more
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FAQ
”I have reported my medical device in the IFA database. Do I also have to register it in EUDAMED? | Yes, because your product data will not be forwarded to EUDAMED by IFA GmbH.“ more
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FAQ
”What is EUDAMED? | The EU Commission shall set up a central database (EUDAMED) for medical devices according to Article 28 MDR.“ more
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FAQ
”Do clinic packs need to be verified? | Yes, clinic packs of medicinal products obliged to verification must be verified.“ more
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FAQ
”Can I notify a UN-Nummer for my product even though it does not have a Sicherheitsdatenblatt (safety data sheet)? | Yes, if the product is a hazardous substance.“ more
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FAQ
”How can I report a UDI-DI to the IFA? | IFA GmbH has implemented a data field in which to report an UDI-DI. The UDI-DI of a different issuing entity can also be entered there.“ more
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FAQ
”Can I choose a PZN? | No, due to the fact that the PZN is a neutral identification key. It is generated automatically.“ more
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FAQ
”In which data format does the IFA provide the information? | The data is output in ASCII format. Given that it is raw data, it first requires programming of the data.“ more
IFA Guide