Catalog Number

4818-60000

Brand Name

Forward

Version/Model Number

4818-60000

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

POQ

Product Code Name

Blood Transfusion Kit

Public Device Record Key

a5d3d437-e8b7-4f25-8a41-d7adfac22698

Public Version Date

September 27, 2021

Public Version Number

1

DI Record Publish Date

September 17, 2021

Package DI Number

00850015884061

Quantity per Package

12

Contains DI Package

00860000925372

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case