Duns Number:301063590
Device Description: ZI-F/ Transpa TI-5 grey
Catalog Number
652080
Brand Name
Creation Willi Geller
Version/Model Number
652080
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"
-
For Single-Use
-
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
K043201
Product Code
EIH
Product Code Name
Powder, Porcelain
Public Device Record Key
2123336d-ee04-43d4-a12c-1f09c4a3c084
Public Version Date
July 24, 2018
Public Version Number
4
DI Record Publish Date
December 06, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 547 |