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Nutrimix

FDA UDI

Class II (US FDA UDI)

by Hospira, Inc.

Identity

Trade Name
Nutrimix FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, non-sterile FDA UDI
Device Name
LATEX-FREE NUTRIMIX MACRO VENTED ADAPTER PIN FDA UDI
Model / Reference
196848 FDA UDI
Description
LATEX-FREE NUTRIMIX MACRO VENTED ADAPTER PIN FDA UDI

Identifiers

Catalog Number
0196848 FDA UDI
Primary DI / UDI-DI
10887787006596 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Enteral feeding kit, adult/paediatric, non-sterile 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

Category: Enteral feeding kit, adult/paediatric, non-sterile

Nutrimix 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, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hospira, Inc.

Sources (1)

  • FDA UDI 4ece557c-c62b-4a07-ba71-3db655509cf8 36 fields · synced Jun 1, 2026