Catalog Number

-

Brand Name

NUVO

Version/Model Number

B2AV800-1

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

FQO

Product Code Name

Table, Operating-Room, Ac-Powered

Public Device Record Key

18723e45-9048-441c-ac43-32e7192afeb3

Public Version Date

September 19, 2022

Public Version Number

2

DI Record Publish Date

January 31, 2020

Package DI Number

01816835022693

Quantity per Package

1

Contains DI Package

00816835022694

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX