Device, unique_device_id says only FDA identifications number should be entered
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Description
See forum discussionhttps://forums.ohdsi.org/t/adding-manufacturer-and-model-information-to-the-device-exposure-table/16561. The unique_device_id column is OK, but the documentation should not be changed.
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First steps
- Read the whole issue, then the project's contributing guide.
- Comment on the issue to say you are picking it up — it saves two people doing the same work.
- Fork the repository and make your change on a branch.
- Open a pull request that references the issue number.
Research direction
Review the linked forum discussion and the issue's statement about unique_device_id; no file or test is identified in the payload. Clarify with a maintainer whether any documentation change is actually requested and define the accepted wording before editing.
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Assessment
- Domain
- documentation
- Issue type
- Documentation
- Difficulty
- 4/5
- Estimated time
- 3-5 days
- Activity status
- Stale
- Clarity
- Needs clarification
- Newbie friendliness
- 25/100