Catalog Number

0910182000

Brand Name

NA

Version/Model Number

0910182000

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 02, 2017

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

DYB

Product Code Name

INTRODUCER, CATHETER

Public Device Record Key

6c6e73ff-4aa8-4e0c-9062-52a59f9f8b26

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2016

Package DI Number

37613252722916

Quantity per Package

20

Contains DI Package

07613252722915

Package Discontinue Date

February 02, 2017

Package Status

Not in Commercial Distribution

Package Type

pack