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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 bijge-
voegde gebruiksaanwijzing op pagina 100 104 nalezen.
Het apparaat is in overeenstemming met de EU-richt-
lijn voor medische hulpmiddelen 93/42/EG, de Duitse
wet inzake medische producten en de normen EN1060-1
(Niet-invasieve bloeddrukmeters deel 1: Algemene eisen),
EN1060-3 (Niet-invasieve bloeddrukmeters deel 3: Aanvul
-
lende eisen voor elektromechanische bloeddrukmeetsys-
temen) en IEC80601-2-30 (Medische elektrische toestellen
deel 2 – 30: Speciale eisen voor basisveiligheid en essenti
-
ele prestaties van niet-invasieve bloeddrukmeters).
De nauwkeurigheid van deze bloeddrukmeter is zorgvul-
dig gecontroleerd en het apparaat is ontwikkeld met het
oog op een lange gebruiksduur. Wanneer het apparaat
wordt gebruikt in de geneeskunde moeten meettechni-
sche controles met daarvoor geschikte middelen worden
uitgevoerd. Uitgebreide informatie voor het controleren
van de nauwkeurigheid kan worden aangevraagd via het
serviceadres.
14


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