Catalog Number

-

Brand Name

Sperm Preparation Medium

Version/Model Number

10702010D

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

K991332,K991332

Product Code

MQL

Product Code Name

Media, Reproductive

Public Device Record Key

5ef7c67f-da56-4385-94e6-1d6ebdd04ffd

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 28, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-