Catalog Number

CER-EXT

Brand Name

CER-EXT

Version/Model Number

11 GA X 6.4 CM

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

K150563,K150563,K150563

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

4b857109-68b6-4d90-94f0-e46f4e1baa4e

Public Version Date

November 17, 2021

Public Version Number

1

DI Record Publish Date

November 09, 2021

Package DI Number

10850023741445

Quantity per Package

1

Contains DI Package

00850023741448

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack