← Back to catalogue

Halyard

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
HALYARD* CORFLO* Nasogastric/Nasointestinal Pediatric Feeding Tube with Stylet FDA UDI
Model / Reference
45764 FDA UDI
Description
HALYARD* CORFLO* Nasogastric/Nasointestinal Pediatric Feeding Tube with Stylet FDA UDI

Identifiers

Catalog Number
20-8226 FDA UDI
Primary DI / UDI-DI
10680651457643 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

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

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI

Category: Nasogastric feeding tube

Halyard 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4f936f6e-f9d7-4239-8e1c-bd8991138922 37 fields · synced Jun 9, 2026