Spectrum IQ

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name: Spectrum IQ FDA UDI
Generic Name: Bedside infusion pump, single-channel FDA UDI
Device Name: The Spectrum IQ Infusion System with Dose IQ Safety Software is an infusion pump that provides delivery of fluids into a patient in a controlled manner. The pumping mechanism is of linear peristaltic design and uses inlet and outlet valves for flow control. The Spectrum IQ infusion pump is specifically manufactured and calibrated for use with Baxter administration sets. FDA UDI
Model / Reference: 3570009 FDA UDI
Description: The Spectrum IQ Infusion System with Dose IQ Safety Software is an infusion pump that provides delivery of fluids into a patient in a controlled manner. The pumping mechanism is of linear peristaltic design and uses inlet and outlet valves for flow control. The Spectrum IQ infusion pump is specifically manufactured and calibrated for use with Baxter administration sets. FDA UDI

Identifiers

Catalog Number: 3570009 FDA UDI
Primary DI / UDI-DI: 00085412610900 FDA UDI
FDA Product Code: PHC FDA UDI
FRN FDA UDI
GMDN Term: Bedside infusion pump, single-channel FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5725 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Bedside infusion pump, single-channel

Spectrum IQ by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Baxter International Inc.

Sources (1)

FDA UDI d161f6ff-ce37-499e-882a-c8c6dc30a53c 36 fields · synced Jun 1, 2026