← Back to catalogue

Norco

FDA UDI

Class II (US FDA UDI)

by North Coast Medical, Inc.

Identity

Trade Name
Norco FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Device Name
Norco Eco-Stim TENS + EMS FDA UDI
Model / Reference
NC89481 FDA UDI
Description
Norco Eco-Stim TENS + EMS FDA UDI

Identifiers

Catalog Number
4123 FDA UDI
Primary DI / UDI-DI
00768627001632 FDA UDI
FDA Product Code
NUH FDA UDI
NGX 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
890.5850 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

Norco by North Coast Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analgesic transcutaneous electrical nerve stimulation system.

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
North Coast Medical, Inc.

Sources (1)

  • FDA UDI 15c57008-c5f5-4a6a-8db4-649d4dbf6314 35 fields · synced May 30, 2026