Catalog Number

-

Brand Name

NC30000T

Version/Model Number

NC30000T

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

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

LRO

Product Code Name

General Surgery Tray

Public Device Record Key

e2742503-4ed9-4f55-acdd-bcb67ceb8c83

Public Version Date

December 04, 2020

Public Version Number

4

DI Record Publish Date

February 19, 2018

Package DI Number

10816336021025

Quantity per Package

5

Contains DI Package

10816336020394

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-