Catalog Number

40-9228

Brand Name

CORFLO Enteral Feeding Tube

Version/Model Number

40-9228

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KNT

Product Code Name

TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Public Device Record Key

f3834c37-db49-4083-a0fc-7e08dde3e1ca

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 24, 2016

Package DI Number

20815149020383

Quantity per Package

10

Contains DI Package

10815149020386

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-