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PadPro

FDA UDI

Class III (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
PadPro FDA UDI
Generic Name
Multifunction cardiac electrode, paediatric FDA UDI
Device Name
PadPro Defib Electrode Pediatric, Radiotranslucent Pads with Medtronic Connector FDA UDI
Model / Reference
2603M FDA UDI
Description
PadPro Defib Electrode Pediatric, Radiotranslucent Pads with Medtronic Connector FDA UDI

Identifiers

Catalog Number
2603M FDA UDI
Primary DI / UDI-DI
10653405042655 FDA UDI
PMA Number
P200004 FDA UDI
510(k) Number
K020288 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Multifunction cardiac electrode, paediatric 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

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

No

FDA UDI

Category: Multifunction cardiac electrode, paediatric

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

Similar devices

Also classified as Multifunction cardiac electrode, paediatric.

Cleared under the same submission

K020288 also covers:

P200004 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI a106a779-5f92-4004-9741-82591127bd41 37 fields · synced May 31, 2026