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Verklaring van de symbolen
c
Bloedglucosemeter: dit product voldoet aan de Europese richtlijn 1999/5/EG betreende
radioapparatuur en telecommunicatie-eindapparatuur (R&TTE).
C
Bloedglucosemeter: dit product voldoet aan de Europese richtlijn 98/79/EG inzake
medische hulpmiddelen voor in-vitrodiagnostiek.
C
Prikpen en lancettenhouder:
deze producten voldoen aan de Europese richtlijn 93/42/EEG inzake medische
hulpmiddelen.
F
Dit apparaat voldoet aan de eisen van deel 15 van de FCC-richtlijnen en van de
standaard RSS-210 van Industry Canada.
Het conformiteitsmerkteken geeft aan, dat het product voldoet aan de eisen van de van
toepassing zijnde norm, en vormt een herleidbare verbinding tussen het apparaat en de
fabrikant, importeur of hun gemachtigde agent, die verantwoordelijk is voor het voldoen
aan de eisen van de norm en voor het op de Australische- en Nieuwzeelandse markt
brengen van het apparaat.
Verklaringen van overige symbolen vindt u in de gebruiksaanwijzingen en bijsluiters van de verschillende
onderdelen van het systeem, die deel uitmaken van de inhoud van de verpakking van de meter.
Conform de richtlijnen van de Continua Health Alliance
Gecertificeerd door het USB Implementers Forum
man_07419341001_04_NL.indb 139 05.12.2016 12:05:04
141


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