Catalog Number

-

Brand Name

Z3

Version/Model Number

3738-930

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

MED

Product Code Name

Sterilant, Medical Devices

Public Device Record Key

731fe56c-ecc4-4272-afe0-d3c116519a11

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2016

Package DI Number

10366975002485

Quantity per Package

4

Contains DI Package

00366975002488

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case