Catalog Number

-

Brand Name

Regard

Version/Model Number

GS00823D

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

LRO

Product Code Name

General Surgery Tray

Public Device Record Key

a4a7df1b-9841-49c9-8ff1-48c410f36094

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

December 10, 2020

Package DI Number

20194717108907

Quantity per Package

25

Contains DI Package

10194717108900

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-