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Hospira

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Hospira FDA UDI
Generic Name
Venous butterfly needle/set FDA UDI
Device Name
LIFESHIELD LATEX-FREE HEMA Y-TYPE BLOOD SET, Nonvented, 100 Inch with Pump and Secure Lock FDA UDI
Model / Reference
1159248 FDA UDI
Description
LIFESHIELD LATEX-FREE HEMA Y-TYPE BLOOD SET, Nonvented, 100 Inch with Pump and Secure Lock FDA UDI

Identifiers

Catalog Number
1159248 FDA UDI
Primary DI / UDI-DI
10887787006862 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Venous butterfly needle/set 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 — 100 Inch FDA UDI

Category: Venous butterfly needle/set

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

Similar devices

Also classified as Venous butterfly needle/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 108ddc2a-4d31-41c4-a544-369749ccce84 37 fields · synced May 30, 2026