Catalog Number

NH221A4

Brand Name

Endure

Version/Model Number

NH221A4-0520

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

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

3d9c4c31-2cb6-4725-a816-005437e0f1ab

Public Version Date

October 06, 2020

Public Version Number

1

DI Record Publish Date

September 28, 2020

Package DI Number

00840118603119

Quantity per Package

100

Contains DI Package

00840118603102

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box