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Lifeshield

FDA UDI

Class II (US FDA UDI)

by Icu Medical Fleet Services, Llc

Identity

Trade Name
Lifeshield FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Primary Microbore PLUM Set 2 CLAVE Y-Sites, Secure Lock, 98 Inch (previously Hospira product) FDA UDI
Model / Reference
1926188 FDA UDI
Description
Primary Microbore PLUM Set 2 CLAVE Y-Sites, Secure Lock, 98 Inch (previously Hospira product) FDA UDI

Identifiers

Catalog Number
1926188 FDA UDI
Primary DI / UDI-DI
10887787008569 FDA UDI
510(k) Number
K141789 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive 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 — 98 Inch FDA UDI

Category: Basic intravenous administration set, noninvasive

Lifeshield by Icu Medical Fleet Services, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 44039392-701e-4cf5-a402-bc913591a7a7 38 fields · synced May 30, 2026