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Powerheart® G3 Pro Rechargeable Battery

FDA UDI

Class III (US FDA UDI)

by Cardiac Science Corporation

Identity

Trade Name
Powerheart® G3 Pro Rechargeable Battery FDA UDI
Generic Name
Secondary battery FDA UDI
Device Name
Rechargeable battery: For Powerheart® AED G3 Pro model 9300P with 1 year full replacement guarantee FDA UDI
Model / Reference
9144-101 FDA UDI
Description
Rechargeable battery: For Powerheart® AED G3 Pro model 9300P with 1 year full replacement guarantee FDA UDI

Identifiers

Catalog Number
9144-101 FDA UDI
Primary DI / UDI-DI
00812394020089 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Secondary battery 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Secondary battery

Powerheart® G3 Pro Rechargeable Battery by Cardiac Science Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secondary battery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardiac Science Corporation

Sources (1)

  • FDA UDI 8901d1bc-1739-4f12-8e45-063d0cabcaa4 34 fields · synced Jun 1, 2026