Catalog Number

-

Brand Name

NUVO

Version/Model Number

B2AV800K-2

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

GDC

Product Code Name

Table, Operating-Room, Electrical

Public Device Record Key

aca6f7e6-ddaa-4539-bbaa-23ebc5c055c4

Public Version Date

September 19, 2022

Public Version Number

2

DI Record Publish Date

January 31, 2020

Package DI Number

01816835022990

Quantity per Package

1

Contains DI Package

00816835022991

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX