← Back to catalogue

CORFLO ULTRA Lite NG

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORFLO ULTRA Lite NG FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
Feeding tube, non weighted FDA UDI
Model / Reference
20-1366AIV FDA UDI
Description
Feeding tube, non weighted FDA UDI

Identifiers

Catalog Number
20-1366AIV FDA UDI
Primary DI / UDI-DI
10815149023134 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 36 Inch FDA UDI
Catheter Gauge — 6 French FDA UDI

Category: Nasogastric feeding tube

CORFLO ULTRA Lite NG by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric feeding tube.

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

Manufacturer
Corpak Medsystems

Sources (1)

  • FDA UDI b981af56-a709-4fc6-b4f0-5670481ef428 36 fields · synced May 31, 2026