Duns Number:300708950
Catalog Number
760116
Brand Name
Ceramill® ZI
Version/Model Number
ZI 31 6pcs.
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 08, 2021
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"
Yes
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
K063511
Product Code
EIH
Product Code Name
Powder, Porcelain
Public Device Record Key
ad9d5f34-967c-42c4-b91a-a625cc4e7f90
Public Version Date
May 10, 2021
Public Version Number
5
DI Record Publish Date
June 30, 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 | 11 |
2 | A medical device with a moderate to high risk that requires special controls. | 1147 |
U | Unclassified | 6 |