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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 Blood Set, 100 mL Burette with Prepierced Additive Port, 170 Micron Filter, Prepierced Secondary Port, Secure Lock, 105 Inch FDA UDI
Model / Reference
1421028 FDA UDI
Description
LIFESHIELD, Primary PLUM Blood Set, 100 mL Burette with Prepierced Additive Port, 170 Micron Filter, Prepierced Secondary Port, Secure Lock, 105 Inch FDA UDI

Identifiers

Catalog Number
1421028 FDA UDI
Primary DI / UDI-DI
10887787006404 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 — 105 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 04e30e9c-3365-4c94-b885-3f0d7d306645 37 fields · synced Jun 8, 2026