Catalog Number

CENT23C

Brand Name

Centros®

Version/Model Number

00884450276235

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

67678289-f932-41fc-b9b7-5166ded29df7

Public Version Date

October 11, 2021

Public Version Number

5

DI Record Publish Date

September 20, 2016

Package DI Number

10884450276232

Quantity per Package

1

Contains DI Package

00884450276235

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-