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Intellisense Adult Defibrillation Pads, CPR Device, Powerheart® G5

FDA UDI

Class II (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
Intellisense Adult Defibrillation Pads,CPR Device, Powerheart® G5 FDA UDI
Generic Name
External defibrillation electrode, adult, single-use FDA UDI
Device Name
Intellisense Adult defibrillation Pads, non-polarized, with CPR Feedback Device for Powerheart® G5 FDA UDI
Model / Reference
XELAED002A FDA UDI
Description
Intellisense Adult defibrillation Pads, non-polarized, with CPR Feedback Device for Powerheart® G5 FDA UDI

Identifiers

Catalog Number
XELAED002A FDA UDI
Primary DI / UDI-DI
00812394020966 FDA UDI
FDA Product Code
LIX FDA UDI
GMDN Term
External defibrillation electrode, adult, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: External defibrillation electrode, adult, single-use

Intellisense Adult Defibrillation Pads, CPR Device, Powerheart® G5 by Zoll Medical Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as External defibrillation electrode, adult, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI a2554ebc-bc39-4cbd-b5d5-bc0d1a35a5e0 36 fields · synced Jun 8, 2026