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Avanos

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
AVANOS FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
CORFLO* Nasogastric/Nasointestinal Feeding Tube FDA UDI
Model / Reference
20-5362 FDA UDI
Description
CORFLO* Nasogastric/Nasointestinal Feeding Tube FDA UDI

Identifiers

Catalog Number
20-5362 FDA UDI
Primary DI / UDI-DI
00350770457420 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric feeding 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 12 Centimeter FDA UDI

Category: Nasogastric feeding tube

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

Similar devices

Also classified as Nasogastric feeding tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI faeeef3e-6aff-40c2-baa4-400d928aa694 36 fields · synced Jun 9, 2026