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Easy@Home Electronic Pain Relief Stimulator Replacement Pads

FDA UDI

Class II (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name
Easy@Home Electronic Pain Relief Stimulator Replacement Pads FDA UDI
Generic Name
Interferential electrical stimulation system electrode FDA UDI
Model / Reference
ETP019 FDA UDI

Identifiers

Primary DI / UDI-DI
00810038634364 FDA UDI
FDA Product Code
NUH FDA UDI
NGX FDA UDI
NYN FDA UDI
IRT FDA UDI
GMDN Term
Interferential electrical stimulation system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5850 FDA UDI
890.5740 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

Category: Interferential electrical stimulation system electrode

Easy@Home Electronic Pain Relief Stimulator Replacement Pads by Easy Healthcare Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Interferential electrical stimulation system electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Easy Healthcare Corporation

Sources (1)

  • FDA UDI 647b7f2b-7988-4cf0-868b-295b512651ba 32 fields · synced May 30, 2026