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136 NL/BE
Dit apparaat voldoet aan de Europese norm EN 60601-1-2
(overeenstemming met CISPR 11, IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-8) en is onderhevig aan bij-
zondere veiligheidsmaatregelen aangaande de elektromag-
netische verdraagzaamheid. Het apparaat is geschikt voor
gebruik in alle omgevingen die in deze gebruiksaanwijzing
worden vermeld, waaronder de thuisomgeving. Houd er
daarbij rekening mee dat draagbare en mobiele HF-com-
municatieinrichtingen dit apparaat kunnen beïnvloeden. Het
apparaat voldoet aan de EU-richtlijn voor medische produc-
ten 93/42/EEC, de wet op medische producten en de nor-
men EN 1060-3 (niet-invasieve bloeddrukmeters deel 3:
aanvullende eisen voor elektromechanische bloeddrukme-
ters) en IEC 80601-2-30 (Medisch elektrische toestellen
deel 2 - 30: Bijzondere bepalingen voor de veiligheid als-
mede voor de essentiële prestaties van geautomatiseerde,
niet-invasieve bloeddrukmeters).
De nauwkeurigheid van deze bloeddrukmeter is zorgvuldig
gecontroleerd en is ontwikkeld met het oog op een lange
gebruiksduur. Bij gebruik van het apparaat in de geneeskunde
moeten meettechnische controles met geschikte middelen
worden uitgevoerd. Precieze gegevens van de controle van
de nauwkeurigheid kunnen via het service-adres worden
aangevraagd.
Hiermee bevestigen wij dat dit product voldoet aan de
Europese RED-richtlijn 2014/53/EU.
136


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