Catalog Number

-

Brand Name

Abdominal Binder

Version/Model Number

4379

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

-

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

FSD

Product Code Name

Binder, Abdominal

Public Device Record Key

dd29e20f-1984-4201-9d9e-a2cb6b2dc757

Public Version Date

September 09, 2021

Public Version Number

1

DI Record Publish Date

September 01, 2021

Package DI Number

00616784437934

Quantity per Package

10

Contains DI Package

00616784437927

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case