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Trackstar 302-11115

by Veridian Healthcare

Trackstar 302-11115 is a Class II device made by Veridian Healthcare, listed in FDA GUDID since 4 Sep 2026 (UDI-DI 00845717012188), registry data as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845717012188 UDI-DI Date4 Sep 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  • Withdrawn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
Trackstar
Generic name
Infrared patient thermometer, ear/skin
Model / reference
302-11115
Primary DI / UDI-DI
00845717012188
FDA product code
SDV
GMDN term
Infrared patient thermometer, ear/skin
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Other devices from Veridian Healthcare

See all devices from Veridian Healthcare →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)