Duns Number:053529939
Catalog Number
X-81813P
Brand Name
DT Illusion X-RO #3 Posts Pkg
Version/Model Number
X-81813P
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 10, 2020
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
ELR
Product Code Name
POST, ROOT CANAL
Public Device Record Key
c88093a9-b6f3-463e-ab13-80a05eb282ce
Public Version Date
September 25, 2020
Public Version Number
3
DI Record Publish Date
November 06, 2018
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 | 335 |
2 | A medical device with a moderate to high risk that requires special controls. | 675 |