Catalog Number

-

Brand Name

IMCO

Version/Model Number

1510-IMC

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

KCT

Product Code Name

Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Public Device Record Key

4aab99fc-0ed5-4b2a-a107-1b8bc84505a1

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

June 20, 2016

Package DI Number

20815842023124

Quantity per Package

5

Contains DI Package

10815842023127

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case