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Medtox® 102520

by Medtox Diagnostics, Inc.

Medtox® 102520 is a Class I device made by Medtox Diagnostics, Inc., listed in FDA GUDID since 31 Mar 2026 (UDI-DI 00690286000742), 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 Number00690286000742 UDI-DI Date31 Mar 2026ListedStatusListed 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  • Withdrawn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
Medtox®
Generic name
Multiple drugs of abuse IVD, control
Model / reference
102520
Primary DI / UDI-DI
00690286000742
FDA product code
DIF
GMDN term
Multiple drugs of abuse IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DIF (Drug Mixture Control Materials).

Other devices from Medtox Diagnostics, Inc.

See all devices from Medtox Diagnostics, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)