Catalog Number

CPA00023

Brand Name

PowerLoc

Version/Model Number

CPA00023

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

41c9bc5d-daf4-4123-8c14-939c0f74d4dc

Public Version Date

October 23, 2019

Public Version Number

3

DI Record Publish Date

June 18, 2016

Package DI Number

10801741117173

Quantity per Package

5

Contains DI Package

00801741117176

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA