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Avanos

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
AVANOS FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
* MIC* Gastrostomy Feeding Tube with ENFit® Connector FDA UDI
Model / Reference
44291 FDA UDI
Description
* MIC* Gastrostomy Feeding Tube with ENFit® Connector FDA UDI

Identifiers

Catalog Number
8100-14LV FDA UDI
Primary DI / UDI-DI
00350770442914 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrostomy 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 14 French FDA UDI

Category: Gastrostomy tube

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

Similar devices

Also classified as Gastrostomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7812e6b9-647d-4a5f-95ee-d6e4bfdd2cc3 36 fields · synced Jun 9, 2026