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Medichoice MST2010

by Owens & Minor Distribution, Inc.

Medichoice MST2010 is a Class II device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 10 Jun 2021 (UDI-DI 10885632120343), 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 Number10885632120343 UDI-DI Date10 Jun 2021ListedStatusListed 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  • Withdrawn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
Medichoice
Generic name
Sputum specimen container IVD
Model / reference
MST2010
Primary DI / UDI-DI
10885632120343
FDA product code
BYZ
GMDN term
Sputum specimen container IVD
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sputum specimen container IVD

Similar devices

Other devices filed under FDA product code BYZ (TRAP, STERILE SPECIMEN).

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)