Duns Number:033505389
Device Description: (POUCH 3.5X9 SELFSEAL)
Catalog Number
SCSA
Brand Name
Advance Dental Products
Version/Model Number
SCSA
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
834841ec-bc87-40a6-83d0-2ce728e8ba70
Public Version Date
November 08, 2019
Public Version Number
2
DI Record Publish Date
February 05, 2019
Package DI Number
20850455007024
Quantity per Package
20
Contains DI Package
10850455007027
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 | 10 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 18 |