Catalog Number

00711202

Brand Name

NA

Version/Model Number

00711202

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 17, 2020

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

KNW

Product Code Name

INSTRUMENT, BIOPSY

Public Device Record Key

24ddc5d6-4417-4436-80a4-877ffaa64c3e

Public Version Date

March 17, 2020

Public Version Number

4

DI Record Publish Date

September 17, 2016

Package DI Number

10816765011420

Quantity per Package

5

Contains DI Package

00816765011423

Package Discontinue Date

March 17, 2020

Package Status

Not in Commercial Distribution

Package Type

Box