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None DSPPSS26DF-5

by Neurovision Medical Products Inc.

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

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 NumberB006PSS26DF52 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
None
Generic Name
Electromyographic needle electrode, single-use
Model / Ref / Catalog
DSPPSS26DF-5
Primary DI / UDI-DI
B006PSS26DF52
FDA Product Code
IKT, ETN
GMDN Term
Electromyographic needle electrode, single-use
Device Class
Class II
Regulation Number
890.1385, 874.1820
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Electromyographic needle electrode, single-useAspiration nerve-locating system probe

Similar devices

Also classified as Aspiration nerve-locating system probe.

Other devices from Neurovision Medical Products Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No