Duns Number:656763489
Catalog Number
-
Brand Name
Silicone Nasal Epistaxis Balloon
Version/Model Number
3101-0830
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EMX
Product Code Name
Balloon, Epistaxis
Public Device Record Key
e772a29d-0743-4d20-9e66-03c0bd8a37eb
Public Version Date
December 02, 2021
Public Version Number
1
DI Record Publish Date
November 24, 2021
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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 307 |
2 | A medical device with a moderate to high risk that requires special controls. | 3 |