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Precisão clínica: De acordo com AAMI-SP10 com referência a
auscultação:
< 5 mmHg compensação sistemática
< 8 mmHg desvio standard
Insuflação: Automático
Esvaziamento: Válvula rítmica
Tipo de pilhas: 2 pilhas tipo LR 03 (AAA)
Temperatura de funcionamento: + 10 °C a + 40 °C
Temperatura de armazenamento: 20 °C a +60 °C
Humidade: Menor de 85% RH
Braçadeira: Diâmetro da braçadeira entre 13 e 21 cm
Avaliação clínica: De acordo com AAMI-SP10 com referência a
auscultação.
(Nota: Esta validação perante métodos intra-
arteriais pode dar lugar a resultados diferentes
aos obtidos com dispositivos validados por
métodos de auscultação.)
Em caso do aparelho não ser utilizado sob as condições de temperatura e humidade
recomendadas, não será assegurada a precisão técnica do mesmo.
Aparelho do tipo BF
Sujeito a modificações sem aviso prévio.
Este aparelho cumpre as seguintes normas:
DIN EN 60601-1: 3/96 «Aparelhos Eléctricos Médicos» –
Parte 1: Requisitos gerais de segurança:
DIN EN 1060-1: 12/95, AMD 1 09/02 «Esfigmomanómetros não invasivos» –
Parte 1: Requisitos gerais:
DIN EN 1060-3: 9/97 «Esfigmomanómetros não invasivos» –
Parte 3: Requisitos suplementares dos sistemas electro-mecânicos de medição
da pressão arterial
Este aparelho cumpre a directiva EC 93 /42 / EEC (Directiva de Aparelho
Médico).
0297
6071360_BP1650_MN_KAZ Seite 52 Donnerstag, 26. Juli 2007 9:45 09
52


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