Catalog Number

CENFP19C

Brand Name

CentrosFLO®

Version/Model Number

00884450199909

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"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

MSD

Product Code Name

Catheter, hemodialysis, implanted

Public Device Record Key

44876e03-beb7-4a4d-871d-f6f5bc9f35ea

Public Version Date

October 11, 2021

Public Version Number

5

DI Record Publish Date

October 31, 2015

Package DI Number

20884450199903

Quantity per Package

5

Contains DI Package

10884450199906

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-