Catalog Number

4033403

Brand Name

Excalibur Introducer System

Version/Model Number

4033403

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

FOZ

Product Code Name

Catheter,intravascular,therapeutic,short-term less than 30 days

Public Device Record Key

eed7c829-f888-44f8-87db-f50137d81649

Public Version Date

June 07, 2019

Public Version Number

3

DI Record Publish Date

February 03, 2017

Package DI Number

10801741074766

Quantity per Package

5

Contains DI Package

00801741074769

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA