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5 Fr Fiber Guide LG1620

by National Advanced Endoscopy Devices, Inc.

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 Number00848657075749 UDI-DI Date12 Oct 2023ListedStatusListed 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  • Withdrawn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
5 Fr Fiber Guide
Generic Name
Laparoscopic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
LG1620
Primary DI / UDI-DI
00848657075749
FDA Product Code
NWV
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, reusable
Device Class
Class I
Regulation Number
884.1720
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Laparoscopic surgical procedure kit, non-medicated, reusable

Other devices from National Advanced Endoscopy Devices, Inc.

See all devices from National Advanced Endoscopy Devices, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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