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00711405

by US Endoscopy

00711405 is a Class II device made by US Endoscopy, listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00816765011546), not in commercial distribution (GUDID) as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816765011546 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Flexible endoscopic cytology brush, single-use
Model / Ref / Catalog
00711405
Primary DI / UDI-DI
00816765011546
FDA product code
FDX
GMDN term
Flexible endoscopic cytology brush, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
Not in Commercial Distribution
Size
Length — 350 Centimeter

Similar devices

Other devices filed under FDA product code FDX (endoscopic cytology brush).

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)