|Type of certification||QSCD | Certification of qualified signature and seal creation devices|
|SRC certificate registration number||SRC.00036.QSCD.09.2020|
|Valid from||29 September 2020|
|Valid until||31 December 2027|
|Certificate holder||idemia Germany GmbH|
|Certified product||Idemia_HC_Germany_NEO_G2.1_HBA, V1|
|Test method||According to article 30 (3) a) of Regulation (EU) No. 910/2014, the certification was done on basis of a Common Criteria Evaluation against the Protection Profiles EN 419211-2:2013, EN 419211-4:2013 and EN 419211-5:2013 which are listed in the Commission Implementing Decision (EU) 2016/650 of 25 April 2016.
The evaluation was performed with Evaluation Assurance Level (EAL) 4+ and assuming an high attack potential (augmentation AVA_VAN.5).
|The audit includes||
|Description||The product “Idemia_HC_Germany_NEO_G2.1_HBA, V1” is a qualified signature device (QSCD). The card is a dual interface card and has a contact-based and a contactless interface.
The product consists (among other things) of the semiconductor (IC) family H13 from Infineon, the card operating system IDEMIA_HC_GERMANY_NEO_G2.1_COS, V1 and an application for the generation of qualified signatures.
The product is an electronic health professional card of the German e-health system. That means, besides the application for the generation of qualified electronic signatures, the card contains additional applications pursuant to requirements from Gematik on the filesystem of electronic health professional cards.
SRC confirms that the product “Idemia_HC_Germany_NEO_G2.1_HBA, V1” of idemia Germany GmbH fulfills the requirements of annex II of Regulation (EU) No. 910/2014 (eIDAS-Regulation) for qualified signature creation devices.