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Easy@Home Self-Adhesive Reusable Electrodes

FDA UDI

Class II (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name
Easy@Home Self-Adhesive Reusable Electrodes FDA UDI
Generic Name
Interferential electrical stimulation system electrode FDA UDI
Model / Reference
ETP101 FDA UDI

Identifiers

Primary DI / UDI-DI
00850253007789 FDA UDI
510(k) Number
K132588 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

Yes

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

Easy@Home Self-Adhesive Reusable Electrodes by Easy Healthcare Corporation — 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

Sources (1)

  • FDA UDI 8d9feb26-d6a7-46f8-bb5c-731d52c4128d 33 fields · synced Jun 8, 2026