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Equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
EQUATE FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Device Name
Pain Therapy TENS & EMS FDA UDI
Model / Reference
WMTTENS-100 FDA UDI
Description
Pain Therapy TENS & EMS FDA UDI

Identifiers

Primary DI / UDI-DI
00194346050055 FDA UDI
510(k) Number
K130723 FDA UDI
FDA Product Code
NUH FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system 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

No

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

Equate by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analgesic transcutaneous electrical nerve stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI b8873103-9d0a-4461-851f-36407fc37b84 34 fields · synced Jun 1, 2026