PadPro

FDA UDI

Class III (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: PadPro FDA UDI
Generic Name: Multifunction cardiac treatment electrode FDA UDI
Device Name: PADPRO Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, Adult/Child greater than 10 kg Radiotransparent Electrode, Anderson/Universal 60" (152 cm) FDA UDI
Model / Reference: 2001-C FDA UDI
Description: PADPRO Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, Adult/Child greater than 10 kg Radiotransparent Electrode, Anderson/Universal 60" (152 cm) FDA UDI

Identifiers

Catalog Number: 2001-C FDA UDI
Primary DI / UDI-DI: 10653405040002 FDA UDI
PMA Number: P200004 FDA UDI
510(k) Number: K014209 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Multifunction cardiac treatment electrode

PadPro by Conmed Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K014209 also covers:

P200004 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI 001f4585-4ebc-4fff-aa26-d23573edab29 37 fields · synced Jun 1, 2026