Duns Number:605440718
Device Description: Magic3™ Antibacterial Hydrophilic Intermittent Catheter, Female
Catalog Number
51514S
Brand Name
Magic3™ Antibacterial Hydrophilic Intermittent Catheter, Female
Version/Model Number
51514S
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"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OHR
Product Code Name
Catheter care tray
Public Device Record Key
c460a313-b105-4694-97c2-4fb9da047aa6
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 26, 2016
Package DI Number
10801741072595
Quantity per Package
50
Contains DI Package
00801741072598
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CA
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 6 |
3 | A medical device with high risk that requires premarket approval | 6 |