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Neuroguard S23-837

by Technomed Engineering B.V.

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 Number08720791375140 UDI-DI Date5 Jun 2026ListedStatusListed 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  • Withdrawn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
Neuroguard
Generic Name
Subdermal needle electrode
Model / Reference
S23-837
Primary DI / UDI-DI
08720791375140
FDA Product Code
IKT, GXZ
GMDN Term
Subdermal needle electrode
Device Class
Class II
Regulation Number
890.1385, 882.1350
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe
Size
Needle Gauge — 30 Gauge
Outer Diameter — 0.3 Millimeter
Length — 22 Millimeter

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Properties

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

Other properties (9)

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