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NOV - Novum IQ

FDA UDI

Class I (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
NOV - Novum IQ FDA UDI
Generic Name
Multiple infusion pump management station FDA UDI
Device Name
Infusion Pump Management unit, mobile FDA UDI
Model / Reference
40700HUB FDA UDI
Description
Infusion Pump Management unit, mobile FDA UDI

Identifiers

Catalog Number
40700HUB FDA UDI
Primary DI / UDI-DI
05413765580895 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Multiple infusion pump management station FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multiple infusion pump management station

NOV - Novum IQ by Baxter Healthcare Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple infusion pump management station.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5ed0f7e-53f5-4d2c-9c8d-bb62e0296064 36 fields · synced Jun 8, 2026