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UnoDose UD45-WHITE-HALLANDALE

by Cordica Medical, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number40813360023644 UDI-DI Date20 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
UnoDose
Generic Name
Medicine cup, single-use
Model / Ref / Catalog
UD45-WHITE-HALLANDALE, 50622
Primary DI / UDI-DI
40813360023644
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

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 (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No