Catalog Number

-

Brand Name

CARDIOXYL ®

Version/Model Number

73P30DS

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K060163,K060163

Product Code

GAT

Product Code Name

SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Public Device Record Key

ca953902-3ec5-4b6f-8761-e3d0c71f1fb2

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

January 09, 2020

Package DI Number

13661522100056

Quantity per Package

12

Contains DI Package

03661522100059

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-