← Back to catalogue

Dual Tab Electrode

FDA UDI

Class II (US FDA UDI)

by Impedimed, Inc.

Identity

Trade Name
Dual Tab Electrode FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Lymphederma Dual Tab Electrodes; each pouch contains 60 single use gel backed electrodes FDA UDI
Model / Reference
292-DTE FDA UDI
Description
Lymphederma Dual Tab Electrodes; each pouch contains 60 single use gel backed electrodes FDA UDI

Identifiers

Catalog Number
292-DTE FDA UDI
Primary DI / UDI-DI
B277292DTE1 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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

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

No

FDA UDI

Category: Electrocardiographic electrode, single-use

Dual Tab Electrode by Impedimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, 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

Manufacturer
Impedimed, Inc.

Sources (1)

  • FDA UDI 982743cb-1d52-467e-8ded-83c5ab7c5ba4 36 fields · synced May 30, 2026