← Back to catalogue

Lifeshield

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Lifeshield FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, sterile FDA UDI
Device Name
LIFESHIELD, Latex-Free, Male/Female Sterile Cap FDA UDI
Model / Reference
1147701 FDA UDI
Description
LIFESHIELD, Latex-Free, Male/Female Sterile Cap FDA UDI

Identifiers

Catalog Number
1147701 FDA UDI
Primary DI / UDI-DI
10887787005148 FDA UDI
FDA Product Code
FPK FDA UDI
GMDN Term
Enteral feeding kit, adult/paediatric, sterile 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

Category: Enteral feeding kit, adult/paediatric, sterile

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

Similar devices

Also classified as Enteral feeding kit, adult/paediatric, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI 55d93ebd-c842-4db5-8399-99b7b6896358 36 fields · synced May 30, 2026