Catalog Number

-

Brand Name

Single Use Aspiration Needle NA

Version/Model Number

NA-411D-1321

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

GAA

Product Code Name

NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

Public Device Record Key

2973cf3f-b2d7-4fdc-834a-1c3cdb764de3

Public Version Date

December 17, 2021

Public Version Number

2

DI Record Publish Date

September 21, 2018

Package DI Number

14953170196703

Quantity per Package

4

Contains DI Package

04953170196706

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-