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T3 Platform Software 2

by Etiometry Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00863061000316 UDI-DIDate17 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
T3 Platform Software
Generic Name
Clinical decision management support software
Model / Reference
2
Primary DI / UDI-DI
00863061000316
FDA Product Code
PLB, PPW
GMDN Term
Clinical decision management support software
Device Class
Class II
Regulation Number
870.2300, 870.2200
GUDID distribution status
In Commercial Distribution

Other devices from Etiometry Inc.

See all devices from Etiometry Inc. →

Properties

  • Manufacturing Date

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No