Catalog Number

-

Brand Name

Regard™

Version/Model Number

UR01150A

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

FDE

Product Code Name

Laparoscopy Kit

Public Device Record Key

03791e58-f685-4ccc-8977-97472fcc7829

Public Version Date

April 14, 2022

Public Version Number

1

DI Record Publish Date

April 06, 2022

Package DI Number

20194717115219

Quantity per Package

4

Contains DI Package

10194717115212

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-