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AED Battery Exchange DBP-1400-ABE

by AED Battery Exchange, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00864312000291 UDI-DI Date15 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
AED Battery Exchange
Generic Name
Primary battery
Model / Reference
DBP-1400-ABE
Primary DI / UDI-DI
00864312000291
PMA Number
FDA Product Code
MKJ
GMDN Term
Primary battery
Device Class
Class III
Regulation Number
870.5310
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (P190013)

Other devices from AED Battery Exchange, LLC

See all devices from AED Battery Exchange, LLC →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

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