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Echelon Flex PLEE45A

by Ethicon Endo-Surgery, LLC

Echelon Flex PLEE45A is a Class II device made by Ethicon Endo-Surgery, LLC, listed in FDA GUDID since 22 Feb 2017 (UDI-DI 10705036015345), 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 Number10705036015345 UDI-DI Date22 Feb 2017ListedStatusListed 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  • Withdrawn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 Flex
Generic name
Endoscopic motorized cutting stapler, single-use
Model / Ref / Catalog
PLEE45A
Primary DI / UDI-DI
10705036015345
FDA product code
GDW
GMDN term
Endoscopic motorized cutting stapler, single-use
Device class
Class II
Regulation number
878.4750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic motorized cutting stapler, single-use

Other devices from Ethicon Endo-Surgery, LLC

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Properties

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