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Natus

FDA UDI

Class II (US FDA UDI)

by Natus Neurology Incorporated

Identity

Trade Name
Natus FDA UDI
Generic Name
Diagnostic peripheral nerve electrical stimulation system FDA UDI
Device Name
ELC/SMALL STIM W/DIN FDA UDI
Model / Reference
019-403800 FDA UDI
Description
ELC/SMALL STIM W/DIN FDA UDI

Identifiers

Primary DI / UDI-DI
00382830040990 FDA UDI
FDA Product Code
IKT FDA UDI
GMDN Term
Diagnostic peripheral nerve electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1385 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Diagnostic peripheral nerve electrical stimulation system

Natus by Natus Neurology Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic peripheral nerve electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Natus Neurology Incorporated

Sources (1)

  • FDA UDI 74747eef-73a5-4f22-b646-a38d2a75df4f 33 fields · synced Jun 9, 2026