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Nerveäna+®

by Neurovision Medical Products Inc. 9 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB600NVPMS2 UDI-DI Date1 Feb 2024ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Nerve-locating system
Primary DI / UDI-DI
B600NVPMS2
FDA Product Code
GWF, ETN
GMDN Term
Nerve-locating system
Device Class
Class II
Regulation Number
882.1870, 874.1820
GUDID distribution status
Not in Commercial Distribution

Other devices from Neurovision Medical Products Inc.

See all devices from Neurovision Medical Products Inc. →

Properties

  • Expiration Date

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Manufacturing Date: No