Catalog Number

41522

Brand Name

Kendall

Version/Model Number

41522

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"

-

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

KDD

Product Code Name

Kit, surgical instrument, disposable

Public Device Record Key

e924f514-1d2b-45c1-9e34-b04deba7a3cd

Public Version Date

November 19, 2020

Public Version Number

3

DI Record Publish Date

June 27, 2018

Package DI Number

20884527018656

Quantity per Package

20

Contains DI Package

10884527018659

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE