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52 Aanvullende informatie
Waarschuwingen
Tekst aangeduid met een
waarschuwingssymbool moet worden gelezen
voordat het product wordt gebruikt.
Fabrikant
Het product is geproduceerd door de
fabrikant waarvan de naam en het
adres naast het symbool vermeld staan.
Dit geeft aan wie de fabrikant van een
medisch apparaat is, zoals vastgelegd in
EU-voorschriften 90/385/EEC, 93/42/EEC en
98/79/EC.
CE-markering
Dit product voldoet aan de Medical Device
Directive 93/42/EEC. Het viercijferige
getal geeft het identicatienummer van de
aangemelde instantie aan.
Elektronisch afval (WEEE)
Recycle uw hoortoestellen, accessoires of
batterijen volgens lokale wetgeving of lever
ze als afval in bij uw hoorzorgprofessional.
Elektronische apparatuur valt onder
Richtlijn 2012/19/EU betreende afval
en elektronische apparatuur (waste and
electrical equipment, WEEE).
E2105
Regulatory Compliance Mark (RCM)
Dit product voldoet aan de eisen voor
elektrische veiligheid, EMC en radiospectrum
voor producten bestemd voor de Australische
of Nieuw-Zeelandse markt.
SN
Serienummer
Geeft het serienummer van de fabrikant
aan zodat een speciek medisch apparaat
geïdenticeerd kan worden.
Beschrijving van symbolen die in dit boekje of op
de verpakking gebruikt worden
52


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