Catalog Number

31410270

Brand Name

Kendall

Version/Model Number

31410270

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 01, 2023

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

FSD

Product Code Name

BINDER, ABDOMINAL

Public Device Record Key

3dcef1a6-0e25-4016-af75-9897815cffb3

Public Version Date

December 14, 2020

Public Version Number

4

DI Record Publish Date

June 23, 2018

Package DI Number

10884527005505

Quantity per Package

50

Contains DI Package

20884527005502

Package Discontinue Date

July 01, 2023

Package Status

In Commercial Distribution

Package Type

CASE