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TDMind

by Technidata

TDMind (TD-MIND-01) is a Class I device made by Technidata, listed in FDA GUDID since 1 Aug 2023 (UDI-DI 03770027519065), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03770027519065 UDI-DI Date1 Aug 2023ListedStatusListed 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  • Withdrawn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

Generic name
Clinical laboratory information system application software
Model / Ref / Catalog
TDMind, TD-MIND-01
Primary DI / UDI-DI
03770027519065
FDA product code
JQP
GMDN term
Clinical laboratory information system application software
Device class
Class I
Regulation number
862.2100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JQP (Calculator/Data Processing Module, For Clinical Use).

Other devices from Technidata

See all devices from Technidata →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)