Catalog Number

06196

Brand Name

Artisan®

Version/Model Number

06196

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"

-

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

-

Product Code

DXX

Product Code Name

System, Catheter Control, Steerable

Public Device Record Key

65262e0e-bdf2-4f04-ab08-7f24d547d748

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2016

Package DI Number

00815671020000

Quantity per Package

6

Contains DI Package

10815671020007

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box