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AED Battery Exchange

FDA UDI

Class III (US FDA UDI)

by AED Battery Exchange, LLC

Identity

Trade Name
AED Battery Exchange FDA UDI
Generic Name
Disposable battery pack FDA UDI
Device Name
Lithium Manganese Dioxide battery for use in Philips(TM) HeartStart(TM) FR3 AED's 861388 and 861389 FDA UDI
Model / Reference
FR3-ABE FDA UDI
Description
Lithium Manganese Dioxide battery for use in Philips(TM) HeartStart(TM) FR3 AED's 861388 and 861389 FDA UDI

Identifiers

Primary DI / UDI-DI
00864312000277 FDA UDI
PMA Number
P190013 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Disposable battery pack FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Disposable battery pack

AED Battery Exchange by AED Battery Exchange, LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Disposable battery pack.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2062fd38-5d17-420b-a1e6-2cc59f82b407 34 fields · synced Jun 1, 2026