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Radiotransparent Defibrillation Electrode 8900-004040-01

by Zoll Medical Corporation

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

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 Number00812394027279 UDI-DI Date29 May 2026ListedStatusListed GUDID: 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  • Withdrawn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
Radiotransparent Defibrillation Electrode
Generic Name
External defibrillation electrode, adult, single-use
Model / Reference
8900-004040-01
Primary DI / UDI-DI
00812394027279
FDA Product Code
MKJ
GMDN Term
External defibrillation electrode, adult, single-use
Device Class
Class III
Regulation Number
870.5310
GUDID distribution status
In Commercial Distribution

Other devices from Zoll Medical Corporation

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Properties

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

Other properties (10)

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