Catalog Number

-

Brand Name

Sporox ® II

Version/Model Number

75190

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 09, 2021

Issuing Agency

In HIBCC

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

MED

Product Code Name

Sterilant, medical devices

Public Device Record Key

113a4711-e192-40da-8eb9-fe90d12bdf0a

Public Version Date

December 09, 2021

Public Version Number

3

DI Record Publish Date

November 24, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-