The Product Categorization structure is defined as Tier 1 > Tier 2 > Tier 3 > product name and manufacturer > model version, which is used to categorize different products or configuration items (CIs) in the BMC Atrium Configuration Management Database (BMC Atrium CMDB).
How to create product categorization in BMC remedy?
On the Product Category tab, click Create. The Product Category Update form appears. Optionally enter or select a Product Type. Select the configuration item (CI) type….To add a product category
In the New Manufacturer dialog box, enter a company.
In the Status field, select Enabled.
What is operational categorization in remedy?
Operational categorization is a three-tier structure that helps you to define the work that is being done for a particular incident, problem, known error, change request, release request, or task.
Why do you need to create product categories?
Product categories represent all of a company’s products that a help desk supports. Each product category must be unique. You might find it helpful to view existing categories before creating new categories. For more information about viewing categories, see Viewing and modifying standard configuration data
What do product categories mean on a help desk?
Product categories represent all of a company’s products that a help desk supports. Each product category must be unique. You might find it helpful to view existing categories before creating new categories.
How to create product categories in Microsoft Office?
From the Standard Configuration tab in the Application Administration Console, select the appropriate company. Click the Create link next to Product Category. The Product Category dialog box is displayed. In the Product Category dialog box, optionally select the Product Type.
How to request a device classification from the FDA?
If you would like a formal device determination or classification from the FDA, consider submitting a 513 (g) Request. For instructions on how to submit a 513 (g) Request, refer to the guidance document “ FDA and Industry Procedures for Section 513 (g) Requests for Information under the Federal Food, Drug, and Cosmetic Act Guidance (2012) .”