Nerveäna+®

FDA UDI

Class II (US FDA UDI)

by Neurovision Medical Products, Inc.

Identity

Trade Name: Nerveäna+® FDA UDI
Generic Name: Electromyographic needle electrode, single-use FDA UDI
Model / Reference: NONE FDA UDI

Identifiers

Catalog Number: DSPNVPFKIT-MF-5 FDA UDI
Primary DI / UDI-DI: B006NVPFKITMF52 FDA UDI
FDA Product Code: IKD FDA UDI
IKT FDA UDI
GMDN Term: Electromyographic needle electrode, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.1175 FDA UDI
890.1385 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

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

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Electromyographic needle electrode, single-use Analytical non-scalp cutaneous electrode

Nerveäna+® by Neurovision Medical Products, Inc. — 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: Neurovision Medical Products, Inc.

Sources (1)

FDA UDI b1bd2c45-b413-4b77-8617-eedfea46cdfd 33 fields · synced Jun 8, 2026