LOINC Code 60560-0: FDA package insert Intended use of the device
60560-0 is a LOINC code used to identify FDA package insert Intended use of the device in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Intended Use of the Device. It is commonly used with the system or sample type ^FDA package insert.
What is this code?
LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Intended Use of the Device. It is commonly used with the system or sample type ^FDA package insert.
When is it used?
- Used in lab systems, EHRs, and clinical data exchange.
- May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
- Status: ACTIVE
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- FDA package insert Intended use of the device
- Intended Use of the Device
- DOCUMENT.REF; FDA insert; Intended use of device; Narrative; Report; SPL; Structured Product Labelling
Where you may see this code
You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.