← Back to catalogue

StemWear

FDA UDI

Class II (US FDA UDI)

by Tensproducts, LLC

Identity

Trade Name
StemWear FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
Conductive pan, 3in. x5in., 2/package FDA UDI
Model / Reference
PLB054-3050 FDA UDI
Description
Conductive pan, 3in. x5in., 2/package FDA UDI

Identifiers

Catalog Number
069 FDA UDI
Primary DI / UDI-DI
B1900691 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Transcutaneous electrical stimulation electrode, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transcutaneous electrical stimulation electrode, single-use

StemWear by Tensproducts, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tensproducts, LLC

Sources (1)

  • FDA UDI a4d764ae-350b-4a9d-8144-daa4ff645a01 34 fields · synced Jun 8, 2026