Halyard

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name: Halyard FDA UDI
Generic Name: Enteral tube tracking system FDA UDI
Device Name: HALYARD CORTRAK 2 Enteral Access System FDA UDI
Model / Reference: 47201 FDA UDI
Description: HALYARD CORTRAK 2 Enteral Access System FDA UDI

Identifiers

Catalog Number: 20-0950 FDA UDI
Primary DI / UDI-DI: 10680651472011 FDA UDI
FDA Product Code: KNT FDA UDI
GMDN Term: Enteral tube tracking system 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Enteral tube tracking system

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

Similar devices

Also classified as Enteral tube tracking system.

CORTRAK 2EAS — Corpak Medsystems · Class II
CORTRAK 2EAS — Corpak Medsystems · Class II
CORTRAK 2EAS — Corpak Medsystems · Class II
CORTRAK 2EAS — Corpak Medsystems · Class II
CORTRAK 2 — Corpak Medsystems · Class II
CORTRAK 2EAS — Corpak Medsystems · Class II
Halyard — Avanos Medical, Inc. · Class II
CORTRAK* 2 ENTERAL ACCESS SYSTEM — Avanos Medical, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Avanos Medical, Inc.

Sources (1)

FDA UDI 5da463d0-8ab1-4743-b08d-6391df1c4f56 35 fields · synced Jun 9, 2026