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Neuroradium

FDA UDI

Class II (US FDA UDI)

by Technomed Engineering B.V.

Identity

Trade Name
Neuroradium FDA UDI
Generic Name
Analytical non-scalp cutaneous lead FDA UDI
Device Name
Disposable Stimulation Clip, Sterile 5-22mm, 10pcs FDA UDI
Model / Reference
NR-4000 FDA UDI
Description
Disposable Stimulation Clip, Sterile 5-22mm, 10pcs FDA UDI

Identifiers

Primary DI / UDI-DI
08720791373573 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Analytical non-scalp cutaneous lead

Neuroradium by Technomed Engineering B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 309333ab-95da-4c60-bc71-4eebb2e1c0de 34 fields · synced May 30, 2026