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15. Belangrijke juridische aanwijzing voor de gebruikervan dit product
Voorvallen die zich wegens storingen van het product voordoen en ernstig lichamelijk letsel veroorzaken, moeten worden gemeld aan
de fabrikant en aan de verantwoordelijke overheidsinstantie in de EU-lidstaat waar de gebruiker zich bevindt.
In de Bondsrepubliek Duitsland zijn dit
de firma Alber GmbH (adres zie achterzijde van deze gebruiksaanwijzing)
het Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM),
Kurt-Georg-Kiesinger-Allee 3
53175 Bonn
www.bfarm.de
In de EU-lidstaten informeert u
uw vertegenwoordiger van Alber GmbH (adres zie achterzijde van deze gebruiksaanwijzing)
de overheidsinstantie die in uw land verantwoordelijk is voor voorvallen met medische hulpmiddelen
Een overzicht van de verantwoordelijke instanties vindt u online op http://ec.europa.eu/growth/sectors/medical-devices/contacts/
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