Catalog Number

CER-SUB-1560

Brand Name

CER-SUB-1560

Version/Model Number

15 GA X 60 MM

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

K131157,K131157,K131157

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

0be93b3d-fe7b-4e96-864e-df8df31adbd4

Public Version Date

October 22, 2021

Public Version Number

1

DI Record Publish Date

October 14, 2021

Package DI Number

10850023741346

Quantity per Package

1

Contains DI Package

00850023741349

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack