Catalog Number

-

Brand Name

Target

Version/Model Number

L FZUSS 0040 R02401 TA

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 03, 2022

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FRL

Product Code Name

Fiber, Medical, Absorbent

Public Device Record Key

91add6e7-1d5b-416e-bc90-2c7fa2d1098b

Public Version Date

January 04, 2022

Public Version Number

2

DI Record Publish Date

February 28, 2020

Package DI Number

10048341011528

Quantity per Package

24

Contains DI Package

00048341011521

Package Discontinue Date

January 03, 2022

Package Status

Not in Commercial Distribution

Package Type

Case