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True Metrix Pro

by Trividia Health, Inc. 9 variants

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 Number10840330705681 UDI-DI Date2 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Glucose monitoring system IVD, home-use
Model / Reference
TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER
Primary DI / UDI-DI
10840330705681
FDA Product Code
NBW
GMDN Term
Glucose monitoring system IVD, home-use
Device Class
Class II
Regulation Number
862.1345
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: TRUE METRIX®

Other devices from Trividia Health, Inc.

See all devices from Trividia Health, Inc. →

Properties

  • Prescription Use
  • Over-the-Counter
  • Lot / Batch Number
  • Serial Number

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No
  • Manufacturing Date: No