Device components and packaging systems must combine to create a product that performs efficiently, safely, and effectively in the hands of the user.
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Hi, I was required to add validation for Material Group 3 (VBAP-MVGR3) in 'Additional Data A' tab (VA01/VA02). In the PAI section, there is a module called 'vbap_bearbeiten'.
In addition, packaging often has a direct function in the application of the treatment; for example, it may act as a fixture or a dispenser.
Therefore, mechanical damage to a package cannot be tolerated.
The package must keep a device sterile throughout all the stresses and hazards generated by the manufacturing, shipping, and storage environments.
Ultimately, any device that is labeled as sterile but arrives nonsterile at the point of use can critically compromise patient safety.
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It explains what platform components you should have functionally working before you begin testing power management during modern standby.
Also included in this section is information about the built-in power management diagnostics in Windows 8.1, and a description of how to use Windows Performance Analyzer (WPA) to observe specific operations during modern standby.