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Cadwell Twisted Disposable Subdermal Needle Electrode 302820-000-100

by Cadwell Industries, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840067101292 UDI-DI Date5 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  • Withdrawn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
Cadwell Twisted Disposable Subdermal Needle Electrode
Generic Name
Subdermal needle electrode
Model / Reference
302820-000-100
Primary DI / UDI-DI
00840067101292
FDA Product Code
GXZ
GMDN Term
Subdermal needle electrode
Device Class
Class II
Regulation Number
882.1350
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Ethylene Oxide
Size
Length — 2.5 Meter

From the manufacturer

Manufacturer's product page: Disposable EEG Cup Electrodes

Other devices from Cadwell Industries, Inc.

See all devices from Cadwell Industries, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No