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Echelon ECH60L

by Ethicon Endo-Surgery, LLC

Echelon ECH60L is a Class II device made by Ethicon Endo-Surgery, LLC, listed in FDA GUDID since 23 Sep 2022 (UDI-DI 10705036034988), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10705036034988 UDI-DI Date23 Sep 2022ListedStatusListed GUDID: 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  • Withdrawn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

Trade name
Echelon
Generic name
Endoscopic motorized cutting stapler, single-use
Model / Ref / Catalog
ECH60L
Primary DI / UDI-DI
10705036034988
FDA product code
GAG
GMDN term
Endoscopic motorized cutting stapler, single-use
Device class
Class II
Regulation number
878.4740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic motorized cutting stapler, single-use

Other devices from Ethicon Endo-Surgery, LLC

See all devices from Ethicon Endo-Surgery, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)