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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
PLUG n' PLAY MODULE FDA UDI
Model / Reference
1239125 FDA UDI
Description
PLUG n' PLAY MODULE FDA UDI

Identifiers

Catalog Number
12391 FDA UDI
Primary DI / UDI-DI
M3351239104251 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

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

Similar devices

Also classified as Bedside infusion pump, single-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI 0ed51e6f-d872-4299-9e5a-bf3eaf778246 37 fields · synced Jun 1, 2026