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Endoscopic Device Classification (Device Use Assessment)

Published: August 9, 2026Updated: August 16, 2026

This test evaluates the type and function of medical devices used during an endoscopic procedure to ensure proper use and safety.

Quick summary

["This assessment helps confirm the correct device was employed during your procedure."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
19783-0
Short code
Endoscopy device Class
Synonyms
Endoscopy device Class
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
5 mL
Stability
Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
4–24 hours
Order
routine

What This Test Measures

This test classifies the endoscopic device used during your procedure, such as whether it was a standard scope, biopsy tool, or specialized instrument. It also checks if the device functioned as intended during the exam. Results may be used to verify compliance with procedural guidelines or to identify any technical issues during the procedure.

Why It Matters During Your Procedure

Proper device classification ensures accurate diagnosis and treatment. If the device was misidentified or malfunctioned, it could affect the quality of the procedure. Your healthcare team may review these results to confirm everything proceeded safely and correctly.

How It’s Performed

This test is not a blood, urine, or tissue sample analysis but rather a review of the device used during your endoscopic procedure. It is typically performed by the endoscopy team during or immediately after the procedure to document device type and function.

Common Uses

Results from this test help verify that the correct device was used for your specific medical need. It may also be used in quality assurance programs to ensure consistent and safe endoscopic practices.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Frequently asked questions

What does this test tell me about my procedure?
This test confirms the type of device used during your endoscopic procedure and ensures it functioned correctly. It does not measure biological samples but helps verify procedural safety and compliance with guidelines.
Will I need to prepare for this test?
No special preparation is needed. This assessment is performed during or right after your endoscopic procedure by the endoscopy team.
Could this test affect my treatment plan?
If findings indicate device issues, your healthcare provider may discuss additional steps or adjustments to your care. Otherwise, this test primarily supports procedural documentation.
  1. 1
    MedlinePlus — Laboratory TestsSource
  2. 2
    Lab Tests OnlineSource
  3. 3
    Mayo Clinic — Tests & ProceduresSource

Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy