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Doselogix TC35 Gold

by Cordica Medical, Inc.

Doselogix TC35 Gold (755174) is a Class I device made by Cordica Medical, Inc., listed in FDA GUDID since 7 Sep 2022 (UDI-DI 00813360022144), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813360022144 UDI-DI Date7 Sep 2022ListedStatusListed 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  • Withdrawn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
Doselogix
Generic name
Medicine cup, single-use
Model / Ref / Catalog
TC35 Gold, 755174
Primary DI / UDI-DI
00813360022144
FDA product code
KYX
GMDN term
Medicine cup, single-use
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Medicine cup, single-use

Similar devices

Other devices filed under FDA product code KYX (Dispenser, Liquid Medication).

Other devices from Cordica Medical, Inc.

See all devices from Cordica Medical, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)