← Back to catalogue

C.M.P. Cable

FDA UDI

Class II (US FDA UDI)

by C.M.P. Canadian Medical Products Inc

Identity

Trade Name
C.M.P. Cable FDA UDI
Generic Name
Interferential electrical stimulation system electrode FDA UDI
Device Name
Pro Carbon IFC Electrodes - 4" Round 1pair FDA UDI
Model / Reference
C5140 FDA UDI
Description
Pro Carbon IFC Electrodes - 4" Round 1pair FDA UDI

Identifiers

Primary DI / UDI-DI
B312C51400 FDA UDI
510(k) Number
K002227 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Interferential electrical stimulation system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

Yes

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

Category: Interferential electrical stimulation system electrode

C.M.P. Cable by C.M.P. Canadian Medical Products Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interferential electrical stimulation system electrode.

Cleared under the same submission

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 2bf1b139-1755-4911-8c0b-b35dca1fb8fc 34 fields · synced Jun 8, 2026