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NeoDevices, Inc.

FDA UDI

Class II (US FDA UDI)

by Neodevices Inc

Identity

Trade Name
NeoDevices, Inc. FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
36" Enteral Extension set with non-IV stepped adapter and enteral only connector FDA UDI
Model / Reference
ND36EO FDA UDI
Description
36" Enteral Extension set with non-IV stepped adapter and enteral only connector FDA UDI

Identifiers

Primary DI / UDI-DI
10816340022056 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Intravenous administration tubing extension set 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intravenous administration tubing extension set

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

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neodevices Inc

Sources (1)

  • FDA UDI 05174111-416f-4671-bf02-c42b8a7f3c9a 34 fields · synced Jun 8, 2026