Catalog Number

-

Brand Name

Enteral Funnel ENFit Transition Connector with cap

Version/Model Number

F00074

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 08, 2019

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"

Yes

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

PIO

Product Code Name

Enteral Specific Transition Connectors

Public Device Record Key

2142677f-c356-4606-b5f9-e8377e6e36b9

Public Version Date

July 23, 2020

Public Version Number

4

DI Record Publish Date

December 28, 2017

Package DI Number

08056093720167

Quantity per Package

24

Contains DI Package

08056093720150

Package Discontinue Date

November 08, 2019

Package Status

Not in Commercial Distribution

Package Type

-