Catalog Number

72626

Brand Name

POWERWAND

Version/Model Number

Pediatric Kit 3Fr X 6cm

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

-

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

-

FDA Premarket Submission

-

Product Code

OWL

Product Code Name

Peripheral Catheter Insertion Kit

Public Device Record Key

818b69d9-1051-4904-896b-e79115ac55b8

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

February 28, 2017

Package DI Number

20859821006449

Quantity per Package

10

Contains DI Package

10859821006442

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box