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© Bosch Healthcare Solutions GmbH 35
Información técnica
Instrucciones de uso
es
Dirección del fabricante Número de referencia / número de
parte de tipo
Este producto DIV cumple con los
requisitos de las Directivas europeas
aplicables.
Tipo de parte aplicable al paciente BF
según EN 60601-1
Leer con cuidado las instrucciones
de uso
Dispositivo médico para diagnós-
tico in vitro según Directiva DIV
98 / 79 / CEE
ADVERTENCIA Observar las advertencias para evitar
situaciones peligrosas
Mantener seco
INFORMATION Aviso importante Clase de protección IP
Fecha de caducidad Compatible con Bluetooth
Exclusivamente para un solo uso Fecha de fabricación
Número de lote Regulatory compliance mark Australia
35


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