Nerveana

FDA UDI

Class II (US FDA UDI)

by Neurovision Medical Products, Inc.

Identity

Trade Name: Nerveana FDA UDI
Generic Name: Nerve-locating system FDA UDI
Model / Reference: N/A FDA UDI

Identifiers

Primary DI / UDI-DI: B006NV0060 FDA UDI
FDA Product Code: GWF FDA UDI
ETN FDA UDI
GMDN Term: Nerve-locating system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1870 FDA UDI
874.1820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Nerve-locating system

Nerveana by Neurovision Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve-locating system.

NIM Vital — MEDTRONIC XOMED, INC. · Class II
Guardian Probe Extension, 4 cm — Checkpoint Surgical, Inc. · Class II
Halyard — Avanos Medical, Inc. · Class II
AVANOS — Avanos Medical, Inc. · Class II
NIM-ECLIPSE® — MEDTRONIC XOMED, INC. · Class II
NIM-Eclipse® — MEDTRONIC XOMED, INC. · Class II
SENTIO — Medos International Sàrl · Class II
Halyard — Avanos Medical, Inc. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Neurovision Medical Products, Inc.

Sources (1)

FDA UDI 1cdf883e-0a02-4287-b60f-36f6db7dff60 32 fields · synced May 30, 2026