IVX Cloud

by Omnicell, Inc. 2 variants

IVX Cloud is a Class II device made by Omnicell, Inc., listed in FDA GUDID since 10 Jan 2024 (UDI-DI 00860006285036), registry data as of 21 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

Source GUDID, synced 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860006285036 UDI-DI	Date10 Jan 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00860006285036

Coverage

1 jurisdiction

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Withdrawn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: 00860006285036
FDA product code: NEP
GMDN term: Intravenous solution compounder

Device class: Class II
Regulation number: 880.5440
GUDID distribution status: In Commercial Distribution

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Class I
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Class II
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Class II
IVX Station Stock Solution Transfer Set Open recall

Class II

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Properties

Single use
Premarket exempt
Serial number
Manufacturing date

Other properties (11, all answered No)