Catalog Number

-

Brand Name

KIMGUARD™ KC500 Sterilization Wrap

Version/Model Number

68130

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

Yes

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

FRG

Product Code Name

Wrap, sterilization

Public Device Record Key

26b6e9d9-cc75-4ab2-9fce-177a6cbc7c09

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

November 30, 2016

Package DI Number

10036000681304

Quantity per Package

2

Contains DI Package

00036000681307

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case