Duns Number:300708950
Catalog Number
760227-STM
Brand Name
Ceramill® ZI
Version/Model Number
ZI 98x20mm
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
fffde4f7-cffd-4a62-898c-39cb77b76428
Public Version Date
November 30, 2020
Public Version Number
4
DI Record Publish Date
December 07, 2017
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 |