Catalog Number

CDC-45552-TTS

Brand Name

ARROW

Version/Model Number

IPN037428

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

K160925,K160925

Product Code

LJS

Product Code Name

Catheter,intravascular,therapeutic,long-term greater than 30 days

Public Device Record Key

04f6c83d-6d5e-4927-ad92-f3f8b55e8daf

Public Version Date

February 19, 2021

Public Version Number

6

DI Record Publish Date

November 15, 2017

Package DI Number

40801902125383

Quantity per Package

3

Contains DI Package

30801902125386

Package Discontinue Date

October 24, 2018

Package Status

Not in Commercial Distribution

Package Type

Case