Catalog Number

CPA00059

Brand Name

PowerLoc

Version/Model Number

CPA00059

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

4fb3ca05-5d3b-4b59-a885-b9a81a7841c9

Public Version Date

October 23, 2019

Public Version Number

2

DI Record Publish Date

November 15, 2018

Package DI Number

10801741182942

Quantity per Package

5

Contains DI Package

00801741182945

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA