AbbVie NJ

FDA UDI

Class II (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name: AbbVie NJ FDA UDI
Generic Name: Nasoenteral tube FDA UDI
Device Name: The AbbVie NJ is a 10 FR, 152 cm, naso-jejunal (NJ) tube made of white radiopaque polyurethane. The AbbVie NJ includes a silicone coated Stylet. The saleable unit (device count) is 1, there are 5 NJs in the saleable unit FDA UDI
Model / Reference: 62903 FDA UDI
Description: The AbbVie NJ is a 10 FR, 152 cm, naso-jejunal (NJ) tube made of white radiopaque polyurethane. The AbbVie NJ includes a silicone coated Stylet. The saleable unit (device count) is 1, there are 5 NJs in the saleable unit FDA UDI

Identifiers

Primary DI / UDI-DI: 38054083008302 FDA UDI
FDA Product Code: KNT FDA UDI
GMDN Term: Nasoenteral tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5980 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Nasoenteral tube

AbbVie NJ by Abbvie Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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NeoMed Enteral Feeding Tube — NEOMED, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Abbvie Inc.

Sources (1)

FDA UDI 4366b3ed-4f49-4e87-9a10-4b9b347ac94c 33 fields · synced May 30, 2026