Catalog Number

-

Brand Name

NA

Version/Model Number

33343

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

BWN

Product Code Name

Table And Attachments, Operating-Room

Public Device Record Key

77603245-2c31-4c90-8ca2-c527f68a8180

Public Version Date

January 20, 2022

Public Version Number

2

DI Record Publish Date

May 06, 2021

Package DI Number

10810050244302

Quantity per Package

1

Contains DI Package

00810050244305

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-