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Chalgren 111-744-24TP

by Chalgren Enterprises, Inc.

Chalgren 111-744-24TP is a Class II device made by Chalgren Enterprises, Inc., listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00816020020146), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816020020146 UDI-DI Date9 Sep 2016ListedStatusListed 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  • Withdrawn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
Chalgren
Generic name
Electromyographic needle electrode, single-use
Model / Ref / Catalog
111-744-24TP
Primary DI / UDI-DI
00816020020146
FDA product code
IKT
GMDN term
Electromyographic needle electrode, single-use
Device class
Class II
Regulation number
890.1385
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization
Size
Needle Gauge — 27 Gauge

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 Chalgren Enterprises, Inc.

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Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)