Catalog Number

CS-12703-E

Brand Name

ARROW

Version/Model Number

IPN030079

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

K862056,K862056

Product Code

DQY

Product Code Name

Catheter, percutaneous

Public Device Record Key

546b9737-3bdf-44af-9cfe-51d0de0d9fa2

Public Version Date

September 23, 2022

Public Version Number

6

DI Record Publish Date

September 21, 2018

Package DI Number

10801902000399

Quantity per Package

5

Contains DI Package

20801902000396

Package Discontinue Date

September 21, 2022

Package Status

Not in Commercial Distribution

Package Type

Case