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Op het verpakkingsmateriaal, het typeplaatje van de meter en de prikpen kunnen de volgende symbolen voorko-
men. De betekenis hiervan is hieronder weergegeven:
Verklaring van de symbolen
Raadpleeg de gebruiksaanwijzing
Waarschuwing (raadpleeg de bijgevoegde
documentatie)! De veiligheidsaanwijzingen
in de gebruiksaanwijzing van het apparaat
raadplegen, a.u.b.
Bewaren bij
Houdbaar tot
Voor eenmalig gebruik
Gesteriliseerd d.m.v. bestraling
Fabrikant
Artikelnummer
Lotnummer
IVD
Voor in vitro diagnostisch gebruik
008
8
Bloedglucosemeter: dit product voldoet
aan de richtlijn 98/79/EG inzake medische
hulpmiddelen voor in-vitro diagnostiek en
aan de richtlijn 1999/5/EG betreffende
radioapparatuur en telecommunicatie-
eindapparatuur (R&TTE).
Prikpen en lancettenhouder: deze produc-
ten voldoen aan de richtlijn 93/42/EEG
inzake medische hulpmiddelen.
Dit apparaat voldoet aan de eisen van deel
15 van de FCC-richtlijnen en van de
standaard RSS-210 van Industry Canada.
Dit apparaat voldoet aan de eisen van de
Japanse radioverkeerwetgeving (”Radio
Law”) 100.
Verklaringen van overige symbolen vindt u in de
gebruiksaanwijzingen/bijsluiters van de verschillende
onderdelen van het systeem, die deel uitmaken van de
inhoud van de verpakking van de meter.
Datum van uitgifte: 2008-11
2


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