Catalog Number

8605RC

Brand Name

Kendall

Version/Model Number

8605RC

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

MMK

Product Code Name

Container, sharps

Public Device Record Key

aac1e6c1-d7d8-4049-b3f7-7da8babc9d07

Public Version Date

February 15, 2019

Public Version Number

7

DI Record Publish Date

June 01, 2017

Package DI Number

10884521513433

Quantity per Package

14

Contains DI Package

20884521513430

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE