Catalog Number

CPA00050

Brand Name

PowerLoc

Version/Model Number

CPA00050

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

6c363185-c21c-40f4-8c12-5e1d4bf00f0f

Public Version Date

October 23, 2019

Public Version Number

2

DI Record Publish Date

September 11, 2018

Package DI Number

10801741175708

Quantity per Package

5

Contains DI Package

00801741175701

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA