Introduction
This manual is a reference for the LOGIQ Book XP Series ultrasound system, applying to all versions of the R2.2.X software.
Regulatory Requirements
The product complies with regulatory requirements of the European Directive 93/42/EEC concerning medical devices and is classified as a Class Ila Medical Device.
The CE label affixed to the product testifies compliance to the Directive, and the location of the CE marking is shown in Chapter 2 of this manual.
Manual:
Download: LOGIQ Book XP Series Basic User Manual
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