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Pro Padz

FDA UDI

Class II (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
PRO PADZ FDA UDI
Generic Name
Rechargeable professional automated external defibrillator FDA UDI
Device Name
PRO*PADZ BIPHASIC MULTI-FUNCTION ELECTRODES - 1 PAIR FDA UDI
Model / Reference
8900-2302-01 FDA UDI
Description
PRO*PADZ BIPHASIC MULTI-FUNCTION ELECTRODES - 1 PAIR FDA UDI

Identifiers

Primary DI / UDI-DI
00847946016418 FDA UDI
FDA Product Code
LDD FDA UDI
GMDN Term
Rechargeable professional automated external defibrillator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5300 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

No

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

No

FDA UDI

Category: Rechargeable professional automated external defibrillator

Pro Padz by Zoll Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rechargeable professional automated external defibrillator.

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 2ab39729-b87d-400d-b5f5-fef9ad150dc6 35 fields · synced Jun 8, 2026