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PadPro

FDA UDI

Class III (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
PadPro FDA UDI
Generic Name
Pin-indexed adaptor, reusable FDA UDI
Device Name
Multifunction Electrode Cable FDA UDI
Model / Reference
EXT10 FDA UDI
Description
Multifunction Electrode Cable FDA UDI

Identifiers

Catalog Number
EXT10 FDA UDI
Primary DI / UDI-DI
10653405046899 FDA UDI
510(k) Number
K003548 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Pin-indexed adaptor, reusable 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pin-indexed adaptor, reusable

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

Similar devices

Also classified as Pin-indexed adaptor, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 7c143177-38f7-4195-a29d-ea00c9e8c406 36 fields · synced Jun 6, 2026