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EZ Trode, 2" x 5" rectangular

FDA UDI

Class II (US FDA UDI)

by Mettler Electronics Corp.

Identity

Trade Name
EZ Trode, 2" x 5" rectangular FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
2" x 5" rectangular electrodes with lead wires, 2 electrodes/pkg. FDA UDI
Model / Reference
2223 FDA UDI
Description
2" x 5" rectangular electrodes with lead wires, 2 electrodes/pkg. FDA UDI

Identifiers

Catalog Number
2223 FDA UDI
Primary DI / UDI-DI
00816864020074 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Transcutaneous electrical stimulation electrode, single-use 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5 Inch FDA UDI

Category: Transcutaneous electrical stimulation electrode, single-use

EZ Trode, 2" x 5" rectangular by Mettler Electronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95d16c47-274b-433c-be84-652e90b1b396 37 fields · synced Jun 6, 2026