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Neuroradium NR-1005

by Technomed Engineering B.V.

Neuroradium NR-1005 is a Class II device made by Technomed Engineering B.V., listed in FDA GUDID since 12 Feb 2024 (UDI-DI 08720791373511), 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 Number08720791373511 UDI-DI Date12 Feb 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Neuroradium
Generic name
Subdermal needle electrode
Model / reference
NR-1005
Description
Disposable Subdermal Needle Electrode corkscrew, 2.5m wire 2x6 colors 12pcs with Protection Cap
Primary DI / UDI-DI
08720791373511
FDA product code
GXZ, IKT
GMDN term
Subdermal needle electrode
Device class
Class II
Regulation number
882.1350, 890.1385
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 2.5 Meter
Outer Diameter — 0.6 Millimeter
Needle Gauge — 23 Gauge

Similar devices in this category

Other devices filed under Subdermal needle electrode.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)