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ElucidVivo A.3

by Elucid Bioimaging, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB745ELUCIDVIVOA3 UDI-DIDate1 Aug 2022ListedStatusListed GUDID: not 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  • Withdrawn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
ElucidVivo
Generic Name
CT system application software
Model / Reference
A.3
Primary DI / UDI-DI
B745ELUCIDVIVOA3
510(k) Number
FDA Product Code
LLZ
GMDN Term
CT system application software
Device Class
Class II
Regulation Number
892.2050
GUDID distribution status
Not in Commercial Distribution

Other devices from Elucid Bioimaging, Inc.

See all devices from Elucid Bioimaging, Inc. →

Properties

Other properties (14)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No