Duns Number:448015938
Device Description: Temporary Material
Catalog Number
559596AN
Brand Name
Systemp.desensitizer
Version/Model Number
559596AN
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 18, 2022
Issuing Agency
In HIBCC
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EMA
Product Code Name
CEMENT, DENTAL
Public Device Record Key
8db1deaa-d110-43c6-a90b-58631dbfca88
Public Version Date
January 19, 2022
Public Version Number
4
DI Record Publish Date
November 10, 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 | 131 |
2 | A medical device with a moderate to high risk that requires special controls. | 12768 |