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TensioMed® Arteriograph24™
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The symbols on the bottom of the device are shown in Figure 2.
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Name of the Manufacturer
6
The name of the device
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The type ID of the device
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The classification of the MDD requirements: II a
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The nominal voltage range applicable with batteries
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The classification of the protection against electric shock
Classification: patient's side: CF.
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Calling the attention to read thoroughly the present User's Manual
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Certification mark guaranteeing that the apparatus complies with the prescriptions
and requirements of the European Union.
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Serial number
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Operating ambient temperature range
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Year of the manufacturing
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Head office of the Manufacturer
17 The permanently placed in unused equipment must be collected in order to get more
efficient reuse and recycling, as well as harmful effects on human health and for the
environment of the ingredients are selectively collected.
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Level of protection against any liquid or grainy material filtering into the device (IP
N
1
N
2
)
N
1
=2: Protected against solid foreign objects of 12,5mm and greater
N
2
=0: Not protected against water
Figure 2.
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