Duns Number:788545692
Catalog Number
002648
Brand Name
Medusa Multi-Coil
Version/Model Number
MMC074-45
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 30, 2017
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
KRD
Product Code Name
Device, Vascular, For Promoting Embolization
Public Device Record Key
3b207689-2d74-44aa-98a6-ccc9302a563f
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
November 02, 2015
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. | 3 |