GI endoscopy devices: terminology and discussion notes
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Yenra | Prepared September 19, 2026
Companion guide: https://yenra.com/olympus-gi-endoscopic-device-line/

Use with the endoscopy team to understand a proposed treatment or clarify equipment documentation. Leave technical choices to trained clinicians and use current local labeling. This sheet is not a device-selection algorithm or a procedure guide.

Keep the completed record privately. This file has no form submission or data collection.

1. Procedure name, date and clinical team:
   ____________________________________________________________

2. Problem or finding the procedure is intended to address:
   ____________________________________________________________

3. Instrument category and its intended role:
   ____________________________________________________________

4. Exact model or product name if relevant to the discussion:
   ____________________________________________________________

5. Current country-specific labeling or patient information supplied:
   ____________________________________________________________

6. How this instrument fits the proposed approach and alternatives:
   ____________________________________________________________

7. Compatibility or single-use/reusable questions for the team:
   ____________________________________________________________

8. Expected benefit and evidence for this condition:
   ____________________________________________________________

9. Important risks and how the team plans follow-up:
   ____________________________________________________________

10. Specimen or pathology results: who explains them and when:
   ____________________________________________________________

11. Discharge instructions and daytime/after-hours contact:
   ____________________________________________________________

12. Question still unresolved and responsible clinician:
   ____________________________________________________________

Source context: use the companion guide and the following primary references to clarify terminology. The responsible team must check current instructions and evidence for the exact equipment or treatment.
https://medical.olympusamerica.com/sites/default/files/us/files/pdf/OAI_ET_0825_CAT_58149_EndoTherapy-Catalog.pdf
https://medical.olympusamerica.com/products/sb-knives
https://medical.olympusamerica.com/procedure/hemostasis
https://content.medical.olympusamerica.com/products/procedure-kits