We are thrilled to announce that the Braillepen24 is now officially certified under the European Medical Device Regulation (MDR). With our official UDI-DI registered 05903754599996, we ensure the highest standards of safety and full compliance for public tenders, professional institutions, and everyday users worldwide.
Please see all details below:
Product name: BraillePen24
Basic UDI-DI: 59037545999BP244F
UDI-DI: 05903754599996
BraillePen24 is an active electronic device intended to compensate for visual impairment by enabling access to and interaction with information through Braille.
Medical device – Class I – Classification rule: Rule 13, Annex VIII, Chapter III of Regulation (EU) 2017/745.
SRN: PL-MF-000055295