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Olympus Endoscopy Kit 345CKETI

by Ruhof Corporation 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10810929045665 UDI-DI Date7 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Olympus Endoscopy Kit
Generic Name
Endoscopy preparation kit
Model / Reference
345CKETI
Primary DI / UDI-DI
10810929045665
FDA Product Code
MNL
GMDN Term
Endoscopy preparation kit
Device Class
Class I
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Other devices from Ruhof Corporation

See all devices from Ruhof Corporation →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No