← Back to catalogue

Powerheart G5 Automatic AED

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
Powerheart G5 Automatic AED FDA UDI
Generic Name
Non-rechargeable public automated external defibrillator FDA UDI
Device Name
Powerheart G5 AED, Fully Automatic, Korean-International English, with Intellisense Adult Pads and Battery FDA UDI
Model / Reference
G5A-19A FDA UDI
Description
Powerheart G5 AED, Fully Automatic, Korean-International English, with Intellisense Adult Pads and Battery FDA UDI

Identifiers

Catalog Number
G5A-19A FDA UDI
Primary DI / UDI-DI
00812394022243 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 Automatic AED by Zoll Medical 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI 6705eb26-9e73-42af-b471-bf17466735f1 36 fields · synced Jun 8, 2026