Catalog Number

-

Brand Name

Regard™

Version/Model Number

HT00271F

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

OES

Product Code Name

Cardiac Catheterization Kit

Public Device Record Key

4e7fb8a2-43d1-4b78-8ede-2094acc069c2

Public Version Date

November 29, 2019

Public Version Number

1

DI Record Publish Date

November 21, 2019

Package DI Number

20194717100307

Quantity per Package

3

Contains DI Package

10194717100300

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-