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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 Pediatric Feeding Tube with Stylet with ENFit® Connector FDA UDI
Model / Reference
40-8368 FDA UDI
Description
CORFLO* Nasogastric/Nasointestinal Pediatric Feeding Tube with Stylet with ENFit® Connector FDA UDI

Identifiers

Catalog Number
40-8368 FDA UDI
Primary DI / UDI-DI
00350770460376 FDA UDI
510(k) Number
K831328 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

Dimensions & Sizes

Size
Length — 8 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2eb95d0a-0759-40f7-9a7f-dd2e4a113f83 37 fields · synced Jun 9, 2026