Catalog Number

A14025060130/A

Brand Name

Advocate™

Version/Model Number

00884450377543

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

LIT

Product Code Name

Catheter, angioplasty, peripheral, transluminal

Public Device Record Key

f908b14b-78a7-4eac-baa8-d25a766fdc4d

Public Version Date

October 11, 2021

Public Version Number

2

DI Record Publish Date

January 31, 2020

Package DI Number

10884450377540

Quantity per Package

10

Contains DI Package

00884450377543

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-