Catalog Number

-

Brand Name

Coaxial needle

Version/Model Number

COX-2000-20-0151

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

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

576a5eb7-1343-4d2f-aa1b-7786957ba9d3

Public Version Date

June 17, 2022

Public Version Number

8

DI Record Publish Date

August 17, 2018

Package DI Number

04260277175238

Quantity per Package

10

Contains DI Package

04260277175108

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-