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Leadpoint 9013C0532

by Natus Manufacturing Limited

Leadpoint 9013C0532 is a Class II device made by Natus Manufacturing Limited, listed in FDA GUDID since 10 Apr 2019 (UDI-DI 00382830053570), 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 Number00382830053570 UDI-DI Date10 Apr 2019ListedStatusListed 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  • Withdrawn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
Leadpoint
Generic name
Electromyographic needle electrode, single-use
Model / Ref / Catalog
9013C0532
Primary DI / UDI-DI
00382830053570
FDA product code
IKD
GMDN term
Electromyographic needle electrode, single-use
Device class
Class II
Regulation number
890.1175
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electromyographic needle electrode, single-use

Similar devices in this category

Other devices filed under Electromyographic needle electrode, single-use.

Other devices from Natus Manufacturing Limited

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Properties

  • Prescription use
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)