Catalog Number

NS-04100-S

Brand Name

ARROW

Version/Model Number

IPN033242

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

K810675,K810675

Product Code

DQX

Product Code Name

WIRE, GUIDE, CATHETER

Public Device Record Key

9a0d38d4-ee9b-48d6-aaac-c6c61bca2792

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

30801902100826

Quantity per Package

5

Contains DI Package

00801902100825

Package Discontinue Date

December 08, 2017

Package Status

Not in Commercial Distribution

Package Type

Case