Catalog Number

-

Brand Name

NUVO PADS

Version/Model Number

B2DCP001709

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

FWZ

Product Code Name

Operating Room Accessories Table Tray

Public Device Record Key

ba56ef21-f7ef-42cb-8d65-8960a3679d13

Public Version Date

September 19, 2022

Public Version Number

2

DI Record Publish Date

March 31, 2020

Package DI Number

01816835023423

Quantity per Package

1

Contains DI Package

00816835023424

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box