Catalog Number

-

Brand Name

Regard™

Version/Model Number

AN00211L

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

OKE

Product Code Name

Port Introducer Kit

Public Device Record Key

69c238eb-a323-4852-958f-9bd512679439

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

April 30, 2020

Package DI Number

20194717107498

Quantity per Package

4

Contains DI Package

10194717107491

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-