Duns Number:034774488
Catalog Number
-
Brand Name
JETi Thrombectomy System, Sterile Disposable Components Kit
Version/Model Number
WV6003
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 18, 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"
-
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
-
Product Code Name
-
Public Device Record Key
a903032c-61b7-48ca-aea5-e62ede9ba83d
Public Version Date
September 27, 2022
Public Version Number
3
DI Record Publish Date
February 08, 2019
Package DI Number
B139WV60032
Quantity per Package
5
Contains DI Package
B139WV60031
Package Discontinue Date
February 18, 2021
Package Status
Not in Commercial Distribution
Package Type
Corrugated Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 39 |