Duns Number:184200736
Device Description: Cannula 5cm, 5mm Tip, 21G
Catalog Number
-
Brand Name
cannulaEchoVU
Version/Model Number
CC5521VU
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 13, 2020
Issuing Agency
In GS1
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
GXI
Product Code Name
Probe, Radiofrequency Lesion
Public Device Record Key
ae651f5e-8462-44d8-8668-0d32031fc330
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
October 20, 2016
Package DI Number
08132500159802
Quantity per Package
10
Contains DI Package
08132500160174
Package Discontinue Date
August 13, 2020
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 10 |