Duns Number:485262658
Catalog Number
-
Brand Name
Auria™ PowerCel™ Charger
Version/Model Number
CI-5600-003
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P960058
Product Code
MCM
Product Code Name
IMPLANT, COCHLEAR
Public Device Record Key
572c4b67-1310-46ef-902a-2ba66d2b047f
Public Version Date
February 06, 2020
Public Version Number
4
DI Record Publish Date
October 08, 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 |
---|---|---|
3 | A medical device with high risk that requires premarket approval | 842 |