Duns Number:057728685
Device Description: (SANI-ROLL 2"-200 M,8/CS)
Catalog Number
SCT2200
Brand Name
Crosstex International
Version/Model Number
SCT2200
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)
-
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
b75055bf-fc77-454d-aece-6706523c7f8d
Public Version Date
November 08, 2019
Public Version Number
3
DI Record Publish Date
November 11, 2016
Package DI Number
50732224109805
Quantity per Package
8
Contains DI Package
10732224109807
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 33 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 25 |