← Back to catalogue

Medi-Trace Cadence

FDA UDI

Class III (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Medi-Trace Cadence FDA UDI
Generic Name
Electrode conductive skin pad, single-use FDA UDI
Device Name
Medi-Trace Cadence Adult, Defibrillation electrode -RTS (10 PR/PK) - Physio-Control FDA UDI
Model / Reference
22550R FDA UDI
Description
Medi-Trace Cadence Adult, Defibrillation electrode -RTS (10 PR/PK) - Physio-Control FDA UDI

Identifiers

Catalog Number
22550R- FDA UDI
Primary DI / UDI-DI
20192253017585 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Electrode conductive skin pad, single-use 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: Electrode conductive skin pad, single-use

Medi-Trace Cadence by Cardinal Health 200, LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive skin pad, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1e2d393b-50ed-4a4a-a059-5479864a9381 34 fields · synced Jun 8, 2026