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NeoConnect Enteral Extension Set

FDA UDI

Class II (US FDA UDI)

by Neomed, Inc.

Identity

Trade Name
NeoConnect Enteral Extension Set FDA UDI
Generic Name
Nasoenteral tube FDA UDI
Device Name
NeoConnect 30” (76 cm) Enteral Extension Set with ENFit Connector, Orange FDA UDI
Model / Reference
EXT-30NC FDA UDI
Description
NeoConnect 30” (76 cm) Enteral Extension Set with ENFit Connector, Orange FDA UDI

Identifiers

Catalog Number
EXT-30NC FDA UDI
Primary DI / UDI-DI
00817584011953 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

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: Nasoenteral tube

NeoConnect Enteral Extension Set by Neomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasoenteral tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neomed, Inc.

Sources (1)

  • FDA UDI 2440f661-ead0-41c4-9d35-f3dcb570b79f 35 fields · synced May 30, 2026