Catalog Number

72202466

Brand Name

N/A

Version/Model Number

72202466

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 14, 2016

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"

Yes

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

FWZ

Product Code Name

Accessories, operating-room, table (kit)

Public Device Record Key

f24f3d0f-0912-4dcb-96ed-e6c97c892d2b

Public Version Date

November 06, 2020

Public Version Number

4

DI Record Publish Date

April 12, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-