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Pro-Padz Radiotransparent

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
Pro-Padz Radiotransparent FDA UDI
Generic Name
Multifunction cardiac treatment electrode FDA UDI
Device Name
Pro-Padz Radiotransparent Solid Gel Electrode Single FDA UDI
Model / Reference
8900-0051-40 FDA UDI
Description
Pro-Padz Radiotransparent Solid Gel Electrode Single FDA UDI

Identifiers

Primary DI / UDI-DI
00847946018337 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Multifunction cardiac treatment electrode 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Multifunction cardiac treatment electrode

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

Similar devices

Also classified as Multifunction cardiac treatment electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f00b1c6-1984-48f0-883c-f2bc6b06e975 34 fields · synced Jun 8, 2026