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EZ Trode, 2.75" round 2222

by Mettler Electronics Corp.

EZ Trode, 2.75" round 2222 is a Class II device made by Mettler Electronics Corp., listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00816864020036), 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 Number00816864020036 UDI-DI Date15 Sep 2016ListedStatusListed 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  • Withdrawn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
EZ Trode, 2.75" round
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / Ref / Catalog
2222
Primary DI / UDI-DI
00816864020036
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 2.75 Inch

Similar devices

Other devices filed under FDA product code GXY (ELECTRODE, CUTANEOUS).

Other devices from Mettler Electronics Corp.

See all devices from Mettler Electronics Corp. →

Properties

  • Over-the-counter
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)