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MicroScan V4.42

by Beckman Coulter, Inc. 4 variants

MicroScan V4.42 is a Class I device made by Beckman Coulter, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 15099590676872), 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 Number15099590676872 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
MicroScan
Generic name
Microorganism identification/antimicrobial-susceptibility analyser IVD
Model / reference
V4.42
Primary DI / UDI-DI
15099590676872
FDA product code
OUG, LON
GMDN term
Microorganism identification/antimicrobial-susceptibility analyser IVD
Device class
Class I
Regulation number
880.6310, 866.1645
GUDID distribution status
In Commercial Distribution

Related devices

Category: Microorganism identification/antimicrobial-susceptibility analyser IVD

Other devices from Beckman Coulter, Inc.

See all devices from Beckman Coulter, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)