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IVX Cloud

by Omnicell, Inc. 2 variants

IVX Cloud is a Class II device made by Omnicell, Inc., listed in FDA GUDID since 25 Jun 2021 (UDI-DI 00860006285029), not in commercial distribution (GUDID) as of 21 Oct 2026.

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

Source GUDID, synced 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860006285029 UDI-DI Date25 Jun 2021ListedStatusListed GUDID: not 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  • Withdrawn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

Generic name
Intravenous solution compounder
Model / reference
IVX Cloud
Primary DI / UDI-DI
00860006285029
FDA product code
NEP
GMDN term
Intravenous solution compounder
Device class
Class II
Regulation number
880.5440
GUDID distribution status
Not in Commercial Distribution

Other devices from Omnicell, Inc.

See all devices from Omnicell, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)