Catalog Number

-

Brand Name

Enteral distal end ENFit Transition Connector

Version/Model Number

7149 00

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"

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

bb327f4c-5f8d-4390-9ed3-6a8c4d56b453

Public Version Date

July 23, 2020

Public Version Number

4

DI Record Publish Date

August 20, 2019

Package DI Number

08056093720723

Quantity per Package

5

Contains DI Package

08056093720716

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-