1 Introduction
18
About the EU Directives
If applicable, your facility’s security strategy should include the practices set forth in the Directive on
the protection of individuals with regard to the processing of personal data and on the free movement
of such data (Directive 95/46/EC of the European Parliament and of the Council of
24 October 1995). In addition, your facility should also take into account any additional, more
stringent standards put forward by any individual EU countries; that is, Germany, France, and so on.
Philips Product Security Policy Statement
Additional security and privacy information can be found on the Philips product security web site at:
http://www.healthcare.philips.com/main/support/equipment-performance/product-security/
index.wpd
Manufacturer Disclosure Statement for Medical Device Security – MDS2
You can view the Manufacturer Disclosure Statements for Medical Device Security (MDS
2
) for
specific devices at:
http://www.healthcare.philips.com/main/support/equipment-performance/product-security/
index.wpd
Overview of System Components
The Avalon CL system consists of the Avalon CL base station, the Avalon CL transducers, the
Avalon CL Fetal & Maternal Pod, the CL Wide Range Pod, and the IntelliVue CL Pods.
The IntelliVue CL Pods are only used for maternal measurements within the Avalon CL solution.
The following table provides an overview of all the devices.
Avalon FM20/FM30 and FM40/
FM50
Wired Transducers
Avalon CL Base Station
Avalon CL Transducers
CL Pods
FM20/FM30
M2702A and M2703A
FM40/FM50
M2704A and M2705A
Avalon CL Base Station
866074
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