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Control™ Meter Kit IGM-0009

by U.S. Diagnostics Inc.

Control™ Meter Kit IGM-0009 (IGM-G3-103) is a Class II device made by U.S. Diagnostics Inc., listed in FDA GUDID since 26 Oct 2017 (UDI-DI 00885502001041), 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 Number00885502001041 UDI-DI Date26 Oct 2017ListedStatusListed 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  • Withdrawn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
Control™ Meter Kit
Generic name
Glucose monitoring system IVD, home-use
Model / Ref / Catalog
IGM-0009, IGM-G3-103
Primary DI / UDI-DI
00885502001041
FDA product code
CGA, NBW
GMDN term
Glucose monitoring system IVD, home-use
Device class
Class II
Regulation number
862.1345
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 1 Microliter

Similar devices

Other devices filed under FDA product code CGA (Glucose Oxidase, Glucose).

Other devices from U.S. Diagnostics Inc.

See all devices from U.S. Diagnostics Inc. →

Properties

  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)