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Lifeshield

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Lifeshield FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
CONTINUUM LIFESHIELD LATEX-FREE PRIMARY I.V. SET, Convertible Piercing Pin, 111 Inch with Removable 3-Port Pressure Activated Valve Manifold, 4-Way High-Flow Stopcock, Backcheck Valve and 2 Prepierced Injection Sites Piggyback with OPTION-LOK FDA UDI
Model / Reference
1911148 FDA UDI
Description
CONTINUUM LIFESHIELD LATEX-FREE PRIMARY I.V. SET, Convertible Piercing Pin, 111 Inch with Removable 3-Port Pressure Activated Valve Manifold, 4-Way High-Flow Stopcock, Backcheck Valve and 2 Prepierced Injection Sites Piggyback with OPTION-LOK FDA UDI

Identifiers

Catalog Number
1911148 FDA UDI
Primary DI / UDI-DI
10887787007593 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 — 111 Inch FDA UDI

Category: Electric infusion pump administration set, single-use

Lifeshield 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 93e8f82d-7e64-4cc4-9468-cf970ad1216e 37 fields · synced May 30, 2026