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Powerheart G5 Kit, Auto, US Eng/ESP LA

FDA UDI

Class III (US FDA UDI)

by Cardiac Science Corporation

Identity

Trade Name
Powerheart G5 Kit, Auto, US Eng/ESP LA FDA UDI
Generic Name
Non-rechargeable public automated external defibrillator FDA UDI
Device Name
Powerheart G5 AED, Fully Automatic, Dual Language (English/Spanish),no battery or pads FDA UDI
Model / Reference
G5A-80P0 FDA UDI
Description
Powerheart G5 AED, Fully Automatic, Dual Language (English/Spanish),no battery or pads FDA UDI

Identifiers

Catalog Number
G5A-80P0 FDA UDI
Primary DI / UDI-DI
00812394020577 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Non-rechargeable public automated external defibrillator 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-rechargeable public automated external defibrillator

Powerheart G5 Kit, Auto, US Eng/ESP LA by Cardiac Science Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rechargeable public automated external defibrillator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0404f83-41d7-43c4-b274-0ee68bb5db1c 36 fields · synced Jun 8, 2026