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: LIFESHIELD LATEX-FREE PLUMSET CONVERTIBLE PIERCING PIN, 110 INCH 2 CLAVE PORTS CLAVE SECONDARY PORT & OPTION-LOK FDA UDI
Model / Reference: 1955738 FDA UDI
Description: LIFESHIELD LATEX-FREE PLUMSET CONVERTIBLE PIERCING PIN, 110 INCH 2 CLAVE PORTS CLAVE SECONDARY PORT & OPTION-LOK FDA UDI

Identifiers

Catalog Number: 1955738 FDA UDI
Primary DI / UDI-DI: 10887787008873 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Bedside infusion pump, single-channel FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 110 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 17cfb5af-8518-4164-83bf-d2548a6fe197 37 fields · synced Jun 6, 2026