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Avcoo

FDA UDI

Class II (US FDA UDI)

by Adp Health Limited

Identity

Trade Name
AVCOO FDA UDI
Generic Name
Interferential electrical stimulation system electrode FDA UDI
Device Name
The Adhesive Electrodes are intended for use as a reusable, conductive adhesive interface between the patient’s skin and the marketed electrical stimulators (i.e. TENS (Transcutaneous Electrical Nerve Stimulation), EMS (Electrical Muscular Stimulation), IF (Interferential) or PGF (Pulsed Galvanic Stimulation) for transmitting electrical current. The electrode is for OTC (Over-The-Counter) or Prescription use. FDA UDI
Model / Reference
EB2010 FDA UDI
Description
The Adhesive Electrodes are intended for use as a reusable, conductive adhesive interface between the patient’s skin and the marketed electrical stimulators (i.e. TENS (Transcutaneous Electrical Nerve Stimulation), EMS (Electrical Muscular Stimulation), IF (Interferential) or PGF (Pulsed Galvanic Stimulation) for transmitting electrical current. The electrode is for OTC (Over-The-Counter) or Prescription use. FDA UDI

Identifiers

Catalog Number
EB2010C21 FDA UDI
Primary DI / UDI-DI
00860012809837 FDA UDI
510(k) Number
K160138 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

Yes

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: Interferential electrical stimulation system electrode

Avcoo by Adp Health Limited — 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

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Manufacturer

Manufacturer
Adp Health Limited

Sources (1)

  • FDA UDI f674b946-0c22-4ce5-833b-71ebdc01f1a5 35 fields · synced Jun 6, 2026