← Back to catalogue

Relief Combo

FDA UDI

Class II (US FDA UDI)

by Neurotron Medical, Inc.

Identity

Trade Name
Relief Combo FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
TENS-EMS device FDA UDI
Model / Reference
PLB043-5010 FDA UDI
Description
TENS-EMS device FDA UDI

Identifiers

Primary DI / UDI-DI
B1870240 FDA UDI
FDA Product Code
IPF FDA UDI
GZJ FDA UDI
GMDN Term
Transcutaneous electrical stimulation electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5850 FDA UDI
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

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transcutaneous electrical stimulation electrode, single-use

Relief Combo by Neurotron Medical, Inc. — 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
Neurotron Medical, Inc.

Sources (1)

  • FDA UDI 33f72cea-6fe0-4c48-99bf-a70e142488f5 33 fields · synced May 30, 2026