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Plum

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Plum FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
LIFESHIELD, Primary PLUM MICRODRIP 150 mL Burette Set, CLAVE Injection Site, 2 CLAVE Y-Sites, Secure Lock, 124 Inch FDA UDI
Model / Reference
1194802 FDA UDI
Description
LIFESHIELD, Primary PLUM MICRODRIP 150 mL Burette Set, CLAVE Injection Site, 2 CLAVE Y-Sites, Secure Lock, 124 Inch FDA UDI

Identifiers

Catalog Number
1194802 FDA UDI
Primary DI / UDI-DI
10887787005179 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electric infusion pump administration set, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 124 Inch FDA UDI

Category: Electric infusion pump administration set, single-use

Plum by Hospira, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI ae58abdd-9355-4ad1-bd60-4a67d1368a3c 37 fields · synced Jun 8, 2026