Catalog Number

PRTSOLO-20

Brand Name

Portico Solo™

Version/Model Number

PRTSOLO-20

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 02, 2017

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

DYB

Product Code Name

INTRODUCER, CATHETER

Public Device Record Key

7f96af4c-2255-450a-a28b-a34a331b9ff8

Public Version Date

June 07, 2019

Public Version Number

3

DI Record Publish Date

April 27, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-