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Additive

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Additive FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
LATEX-FREE ADDITIVE HINGE CAP LifeCare Flexible Container FDA UDI
Model / Reference
485801 FDA UDI
Description
LATEX-FREE ADDITIVE HINGE CAP LifeCare Flexible Container FDA UDI

Identifiers

Catalog Number
0485801 FDA UDI
Primary DI / UDI-DI
10887787001874 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Basic intravenous administration set, noninvasive

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

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI 3710fa68-36fa-4ad4-923e-eb33daa027fe 36 fields · synced May 30, 2026