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Dragonfly® DSPSCKIT-MT-5

by Neurovision Medical Products Inc.

Dragonfly® DSPSCKIT-MT-5 is a Class II device made by Neurovision Medical Products Inc., listed in FDA GUDID since 20 Apr 2023 (UDI-DI B006SCKITMT52), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB006SCKITMT52 UDI-DI Date20 Apr 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dragonfly®
Generic name
Nerve-locating system probe, single-use
Catalogue number
DSPSCKIT-MT-5
Primary DI / UDI-DI
B006SCKITMT52
FDA product code
ETN, GXZ, IKT
GMDN term
Nerve-locating system probe, single-use
Device class
Class II
Regulation number
874.1820, 882.1350, 890.1385
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electromyographic needle electrode, single-useNerve-locating system probe, single-useElectromyographic endotracheal tube electrode

Other devices from Neurovision Medical Products Inc.

  • Dsprlnkit-M-5 Open recall

    Class II

  • Dsprlnkit-Lt-5 Open recall

    Class II

  • Dsprlnkit-St-5 Open recall

    Class II

  • Dsprlnkit-Mt-5 Open recall

    Class II

See all devices from Neurovision Medical Products Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)