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HomeIFA for Data RecipientsNew customersIFA information service – sample products

IFA information service – sample products

”Sample product 10228 is a data stock product i e it contains all data available in the IFA Database at the observation date Sample product 20228 is an update product It contains all new entries changes and deletions in the observation period Both products contain“ ... more

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FAQ

”What clear print requirements are there for German-Austrian multi market packs? | As for single market packs, the four elements of the unique identifier (UI) must be affixed in clear print adding the nationally predefined label. Please pay attention to the requirments of“ ... more

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FAQ

”Do all physician samples have to bear a PZN from 09.02.2019? | Ärztemuster according to article 96 of the regulation 2001/83/EG must bear the security features according delegated act (EU) 2016/161 (article 2 and 41).A frequent question is how the samples need to be“ ... more

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FAQ

”Should I register a stiftung ear Registrierungsnummer (WEEE-Reg.-Nr. DE) for all electric appliances? | Yes, all products listed with “ja” in the following attributes should be registered with a Registrierungsnummer: ElektroStoffV: yes underlies regulation“ ... more

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FAQ

”Does the supplier need to notify the Battery registration number by stiftung ear to IFA? | Please notify your product’s Battery registration number by stiftung ear for publication in the IFA database if the following applies: You are supplier of a product with a“ ... more

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FAQ

”How do single market packs and multi market packs have to be marked with and without blue box? | Single Market Packs (SMP) without Blue Box: According to dVO, the product code must be affixed close to the Data Matrix Codes. Germany permits PPN or NTIN as product codes.“ ... more

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FAQ

”From what point in time do I need to mark my medical device with a UDI-DI? | Depending on the class of the medical devices, the UDI carriers must be placed on the label within one to 5 years from 26.05.2021 according to Article 123 (3) point f MDR. See FAQ No 6. of EC's“ ... more

HomeIFA Coding SystemUnique Device Identification (UDI)

Unique Device Identification (UDI)

”A worldwide system for unique identification of medical devices is introduced with European regulation EU 2017 745 on medical devices and EU 2017 746 on in vitro diagnostics IVDR It is based on the UDI unique device identifier a generic term for product“ ... more

HomeIFA Coding SystemCodes for transport logistics

Codes for transport logistics

”IFA GmbH provides its customers with all necessary elements needed for uniquely and standardized marking of shipping units both the basic shipping label and the expanded label are based on EU standards EN 1573 bar coding – multi industry transport label and“ ... more

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FAQ

”Does the PZN have to be in the Data Matrix Code as fifth element? | No, since the PZN is embedded in both PPN and NTIN, there is no need in Germany to encode it as further (fifth) element. Multi country packs are a specialty because they do not contain the PZN within the“ ... more