Generic Device Data

The Generic Device Data provides the details related to the device identification that is created for a particular medical product.

Required Access Roles:

  • App-specific: Product Manager
  • Baseline: Leader

To access this page:

This topic describes:

This page discusses:

Fields

Field Name Description
Owner The person who is responsible for the DI.
Policy The policy of the object.
State The current state of the object.
Originated The date on which the DI is created.
Modified The date on which the DI was last modified.
DM DI Different from Primary DI Whether the number of DM DI is different from the primary DI. If the number is different, the value is displayed as Yes. Otherwise No.
GMDN Code The unique number identifier, which is used to identify the medical device.
For Single-Use Whether the selected device is created for single or multiple usages. If it is created for the single usage, the value is displayed as Yes. Otherwise No.
Device labeled as Not made with natural rubber latex Whether the device is labeled that it is not made of natural rubber latex. If it is not created using the natural rubber latex, the value is displayed as Yes. Otherwise No.
Device Packaged as Sterile Whether the device is sterilized or not. If it is sterilized while packaging, the value is displayed as Yes. Otherwise No.
Requires Sterilization Prior to Use Whether the device needs to be sterilized before the use or not. If it is require to sterilize before the use, the value is displayed as Yes. Otherwise No.

Actions and Toolbar Commands

Action Description
Edit Lets you edit the details of the generic data of the device. For more information, see Editing Generic Device Data Details.