Duns Number:040469731
Device Description: The SteriScan Bowie Dick Indicator is for exclusive use with the VERIFY All-In-One STEAM R The SteriScan Bowie Dick Indicator is for exclusive use with the VERIFY All-In-One STEAM Reusable Test Pack.
Catalog Number
5500
Brand Name
SteriScan
Version/Model Number
5500
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 11, 2020
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
K120592,K120592
Product Code
JOJ
Product Code Name
Indicator, physical/chemical sterilization process
Public Device Record Key
3af5d566-bf3e-4e20-84f3-5ff21a0310f4
Public Version Date
February 19, 2021
Public Version Number
7
DI Record Publish Date
September 13, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1528 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1557 |