Catalog Number

-

Brand Name

CARDIONYL®

Version/Model Number

721772

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

K913102,K913102

Product Code

GAR

Product Code Name

Suture, nonabsorbable, synthetic, polyamide

Public Device Record Key

a43ca3a5-794f-42cf-bbc1-ff6b279f0e63

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

January 09, 2020

Package DI Number

13661522023829

Quantity per Package

36

Contains DI Package

03661522023822

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-