Catalog Number

-

Brand Name

Stradis Medical, LLC.

Version/Model Number

IMPA1213B

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

FRG

Product Code Name

Wrap, Sterilization

Public Device Record Key

1724f586-9513-4392-bb93-3bf632713e9e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 07, 2017

Package DI Number

M752IMPA1213B5

Quantity per Package

30

Contains DI Package

M752IMPA1213B0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

outer box