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Tracheal Intubation Fiberscope Olympus Lf-Tp

by Olympus Medical Systems Corporation

Listed FDA GUDID listing, not in commercial distribution

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 Number04953170136825 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Tracheal Intubation Fiberscope
Generic Name
Flexible intubation laryngoscope, fibreoptic
Model / Reference
OLYMPUS LF-TP
Primary DI / UDI-DI
04953170136825
FDA Product Code
EOQ
GMDN Term
Flexible intubation laryngoscope, fibreoptic
Device Class
Class II
Regulation Number
874.4680
GUDID distribution status
Not in Commercial Distribution

Other devices from Olympus Medical Systems Corporation

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Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No