Neurosign V4

FDA UDI

Class II (US FDA UDI)

by Technomed Engineering B.V.

Identity

Trade Name: Neurosign V4 FDA UDI
Generic Name: Electromyographic endotracheal tube electrode FDA UDI
Device Name: Lantern Laryngeal Electrode 8/9mm to fit 8 or 9mm Endotracheal Tubes including 2 reusable cables FDA UDI
Model / Reference: 4200-00 FDA UDI
Description: Lantern Laryngeal Electrode 8/9mm to fit 8 or 9mm Endotracheal Tubes including 2 reusable cables FDA UDI

Identifiers

Primary DI / UDI-DI: 08718375865491 FDA UDI
FDA Product Code: ETN FDA UDI
GMDN Term: Electromyographic endotracheal tube electrode FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electromyographic endotracheal tube electrode

Neurosign V4 by Technomed Engineering B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Technomed Engineering B.V.

Sources (1)

FDA UDI 964a62ea-5b93-4fed-9614-ef674e61f826 34 fields · synced Jun 8, 2026