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Powerheart® G3 Pro Battery Charger Kit

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
Powerheart® G3 Pro Battery Charger Kit FDA UDI
Generic Name
Non-rechargeable public semi-automated external defibrillator FDA UDI
Device Name
Charger kit, English, for rechargeable battery: Powerheart AED G3 Pro model 9300P FDA UDI
Model / Reference
9044-001 FDA UDI
Description
Charger kit, English, for rechargeable battery: Powerheart AED G3 Pro model 9300P FDA UDI

Identifiers

Catalog Number
9044-001 FDA UDI
Primary DI / UDI-DI
00812394021345 FDA UDI
510(k) Number
K102496 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Non-rechargeable public semi-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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-rechargeable public semi-automated external defibrillator

Powerheart® G3 Pro Battery Charger Kit by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rechargeable public semi-automated external defibrillator.

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 16bb42ac-886e-4b1b-804c-e84ecdb6fa7e 36 fields · synced Jun 6, 2026