Catalog Number

SSDV20

Brand Name

Steriking®

Version/Model Number

SSDV20

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

K221016,K221016,K221016

Product Code

FRG

Product Code Name

Wrap, Sterilization

Public Device Record Key

ba2e3a4e-0563-45b2-b9b7-a6f19cc633a6

Public Version Date

June 29, 2022

Public Version Number

1

DI Record Publish Date

June 21, 2022

Package DI Number

06438263665522

Quantity per Package

4

Contains DI Package

06438263665515

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-