Plum

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name: Plum FDA UDI
Generic Name: Bedside infusion pump, single-channel FDA UDI
Device Name: Plum A+ Version 13.43 w/MedNet FDA UDI
Model / Reference: 2079225 FDA UDI
Description: Plum A+ Version 13.43 w/MedNet FDA UDI

Identifiers

Catalog Number: 20792 FDA UDI
Primary DI / UDI-DI: M3352079204251 FDA UDI
FDA Product Code: 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

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

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 8 Inch FDA UDI
Height — 8 Inch FDA UDI
Depth — 6 Inch FDA UDI

Category: Bedside infusion pump, single-channel

Plum by Hospira, 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: Hospira, Inc.

Sources (1)

FDA UDI bd904459-02d5-4604-a431-5967c6f6f7be 37 fields · synced May 30, 2026