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YABE Electrode IEC-EE239

by Cynosure, LLC

YABE Electrode IEC-EE239 is a Class II device made by Cynosure, LLC, listed in FDA GUDID since 30 Jan 2017 (UDI-DI 00841494107123), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841494107123 UDI-DI Date30 Jan 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  • Withdrawn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
YABE Electrode
Generic name
Open-surgery electrosurgical electrode, monopolar, reusable
Model / Ref / Catalog
IEC-EE239
Primary DI / UDI-DI
00841494107123
FDA product code
JOS
GMDN term
Open-surgery electrosurgical electrode, monopolar, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Open-surgery electrosurgical electrode, monopolar, reusable

Other devices from Cynosure, LLC

See all devices from Cynosure, LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)