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Hospira

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Hospira FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
250 mL EMPTY CONTAINER FDA UDI
Model / Reference
795112 FDA UDI
Description
250 mL EMPTY CONTAINER FDA UDI

Identifiers

Catalog Number
0795112 FDA UDI
Primary DI / UDI-DI
10887787006855 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

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
Total Volume — 250 Milliliter FDA UDI

Category: Basic intravenous administration set, noninvasive

Hospira 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 ded8e873-b23a-42af-84fe-569a6b4852e0 37 fields · synced Jun 1, 2026