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Adhesive Electrodes 202-496

by Drive Devilbiss Healthcare 2 variants

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 Number00850689007506 UDI-DI Date1 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  • Withdrawn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
Adhesive Electrodes
Generic Name
Transcutaneous electrical stimulation electrode, single-use
Model / Reference
202-496
Primary DI / UDI-DI
00850689007506
FDA Product Code
GXY
GMDN Term
Transcutaneous electrical stimulation electrode, single-use
Device Class
Class II
Regulation Number
882.1320
GUDID distribution status
Not in Commercial Distribution

Other devices from Drive Devilbiss Healthcare

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Properties

  • Lot / Batch Number
  • Expiration Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No