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Auto-Band® DBL-293

by Endochoice, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816849010014 UDI-DI Date8 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  • Withdrawn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
Auto-Band®
Generic Name
Oesophageal endoscopic ligator, single-use
Model / Reference
DBL-293
Primary DI / UDI-DI
00816849010014
FDA Product Code
MND
GMDN Term
Oesophageal endoscopic ligator, single-use
Device Class
Class II
Regulation Number
876.4400
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Single Use
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No