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Lifeshield

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Lifeshield FDA UDI
Generic Name
Burette intravenous administration set FDA UDI
Device Name
LIFESHIELD Primary PLUM MICRODRIP 150 mL Burette Set CLAVE Injection Site, 2 CLAVE Y-Sites, 123 Inch FDA UDI
Model / Reference
1935602 FDA UDI
Description
LIFESHIELD Primary PLUM MICRODRIP 150 mL Burette Set CLAVE Injection Site, 2 CLAVE Y-Sites, 123 Inch FDA UDI

Identifiers

Catalog Number
1935602 FDA UDI
Primary DI / UDI-DI
10887787007661 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Burette intravenous administration set 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

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 — 123 Inch FDA UDI

Category: Burette intravenous administration set

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

Similar devices

Also classified as Burette intravenous administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI b0f0de46-c20a-4ce9-a77e-cefefbc040a4 37 fields · synced May 30, 2026