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TruDenta Earclip Electrode Pad

FDA UDI

Class III (US FDA UDI)

by Electromedical Products International, Inc.

Identity

Trade Name
TruDenta Earclip Electrode Pad FDA UDI
Generic Name
Electrical probe/electrode conductive pad FDA UDI
Device Name
TruDenta Earclip Electrode Pad FDA UDI
Model / Reference
TruDenta Earclip Electrode Pad FDA UDI
Description
TruDenta Earclip Electrode Pad FDA UDI

Identifiers

Primary DI / UDI-DI
00857869005239 FDA UDI
FDA Product Code
JXK FDA UDI
GMDN Term
Electrical probe/electrode conductive pad FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
882.5800 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical probe/electrode conductive pad

TruDenta Earclip Electrode Pad by Electromedical Products International, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical probe/electrode conductive pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d090abc-1825-453f-b78c-49228703f0bd 33 fields · synced Jun 1, 2026