Duns Number:532702946
Device Description: The Comaneci is intended for use in the neurovasculature to assist in the coil embolizatio
Catalog Number
-
Brand Name
Comaneci 17
Version/Model Number
ANPP7199
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
DEN170064,DEN170064,DEN170064,DEN170064
Product Code
PUU
Product Code Name
Temporary Coil Embolization Assist Device
Public Device Record Key
74d854b1-8ef5-487c-ac3c-886ba1801898
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
May 17, 2019
Package DI Number
27290015107154
Quantity per Package
4
Contains DI Package
17290015107157
Package Discontinue Date
-
Package Status
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. | 1 |