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Halyard

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Wearable percutaneous catheter/tube holder FDA UDI
Device Name
HALYARD* CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System FDA UDI
Model / Reference
46905 FDA UDI
Description
HALYARD* CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System FDA UDI

Identifiers

Catalog Number
25-018 FDA UDI
Primary DI / UDI-DI
10680651469059 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Wearable percutaneous catheter/tube holder 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

Category: Wearable percutaneous catheter/tube holder

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

Similar devices

Also classified as Wearable percutaneous catheter/tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f349d413-b01d-4495-95cb-28e8bb3ee9c6 35 fields · synced Jun 9, 2026