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29
Symbol
Explanation
Indicates the compliance with the essential requirements of the Council Directive
93/42/EEC of 14 June 1993 concerning medical devices.
Indicates that the device is a medical device.
Indicates that the part of the appliance that comes into physical contact with the user
(also known as the applied part) is of type BF (Body Floating) according to IEC 60601-1.
The applied part is the breast pump kit.
Indicates 'Class II Equipment'. The adapter is double-insulated (Class II).
Indicates manufacturer's catalog number of the breast pump.
Indicates 'direct current'.
Indicates 'alternating current'.
Indicates separate collection for electrical and electronic equipment in accordance with
the EU directive. Electrical waste products should not be disposed of with household
waste. See chapter 'Recycling' for more information.
Indicates the protection against ingress of solid foreign objects greater than 12.5 mm and
against harmful effects due to the ingress of dripping water when tilted at 15 degrees.
Indicates the protection against ingress of solid foreign objects greater than 12.5 mm and
no protection against ingress of water.
Indicates the batch number of the medical device.
Indicates the manufacturer's serial number of the medical device.
Indicates USB.
Indicates the relative humidity upper limits to which the device can be safely exposed:
up to 90 %.
Indicates the storage and transportation temperature limits to which the medical device
can be safely exposed: ‑25 °C to 70 °C/‑13 °F to 158 °F.
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