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Corpgrip NG/NI tube retention system

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Corpgrip NG/NI tube retention system FDA UDI
Generic Name
Nasogastric tube holder, intranasal FDA UDI
Device Name
CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System FDA UDI
Model / Reference
25-012 FDA UDI
Description
CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System FDA UDI

Identifiers

Catalog Number
25-012 FDA UDI
Primary DI / UDI-DI
00350770005805 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric tube holder, intranasal 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

Yes

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: Nasogastric tube holder, intranasal

Corpgrip NG/NI tube retention system by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric tube holder, intranasal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI 55b347e9-3218-4d3f-a96d-0f7c1daaea2c 35 fields · synced Jun 9, 2026