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Easy@Home Mini Wireless TENS Pulse Stimulator Replacement Pads

FDA UDI

Class II (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name
Easy@Home Mini Wireless TENS Pulse Stimulator Replacement Pads FDA UDI
Generic Name
Neuromuscular transmission electrode FDA UDI
Model / Reference
ETP015 FDA UDI

Identifiers

Primary DI / UDI-DI
00855944007659 FDA UDI
510(k) Number
K141260 FDA UDI
FDA Product Code
NUH FDA UDI
GMDN Term
Neuromuscular transmission electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neuromuscular transmission electrode

Easy@Home Mini Wireless TENS Pulse Stimulator Replacement Pads by Easy Healthcare Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Neuromuscular transmission electrode.

Cleared under the same submission

K141260 also covers:

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 d97d5f3f-49c4-4e6b-9db9-75dc2ae4a27c 33 fields · synced May 30, 2026