Catalog Number

-

Brand Name

Hemoflow™

Version/Model Number

0500154A

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 07, 2018

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

-

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

MSF

Product Code Name

HEMODIALYZER, RE-USE, HIGH FLUX

Public Device Record Key

122cf55f-e3df-4ae5-bbbe-1febd4a26c56

Public Version Date

August 12, 2020

Public Version Number

4

DI Record Publish Date

September 24, 2015

Package DI Number

10840861100061

Quantity per Package

12

Contains DI Package

00840861100064

Package Discontinue Date

August 07, 2018

Package Status

Not in Commercial Distribution

Package Type

-