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Houd er rekening mee dat draagbare en mobiele HF-com-
municatieapparatuur dit apparaat kan beïnvloeden. U kunt
uitgebreide informatie aanvragen bij de klantenservice op het
aangegeven adres of deze aan het eind van de gebruiksaan-
wijzing nalezen.
Het apparaat is in overeenstemming met de EU-richtlijn voor
medische hulpmiddelen 93/42/EEC, de Duitse wet inzake
medische producten en de normen EN1060-1 (Non-invasieve
bloeddrukmeters deel 1: Algemene eisen) en EN1060-3 (Non-
invasieve bloeddrukmeters deel 3: Aanvullende eisen voor
elektromechanische bloeddrukmeetsystemen) en IEC80601-
2-30 (Medische elektrische toestellen deel 2-30: Bijzondere
eisen voor de veiligheid, met inbegrip van essentiële gebruik-
seigenschappen, van automatische non-invasieve bloed-
drukmeters).
De nauwkeurigheid van deze bloeddrukmeter is zorgvuldig
gecontroleerd en het apparaat is ontwikkeld met het oog op
een lange gebruiksduur.
Wanneer het apparaat wordt gebruikt in de geneeskunde
moeten meettechnische controles met daarvoor geschikte
middelen worden uitgevoerd. Uitgebreide informatie voor het
controleren van de nauwkeurigheid kan worden aangevraagd
via het serviceadres.
13


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