Catalog Number

NEZ22034

Brand Name

EZ FLO

Version/Model Number

NEZ22034

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

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

2a32ef13-afc6-4939-b88f-554aa1a4450e

Public Version Date

November 09, 2020

Public Version Number

2

DI Record Publish Date

April 15, 2020

Package DI Number

20850017403141

Quantity per Package

20

Contains DI Package

10850017403144

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE