Duns Number:038000253
Device Description: BREEZE® INTRODUCER KIT
Catalog Number
BINTN
Brand Name
BREEZE® INTRODUCER KIT
Version/Model Number
BINTN
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
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OFL
Product Code Name
Percutaneous sheath introducer kit
Public Device Record Key
d81396c9-a2c5-467e-a14e-b5d1c1cdf780
Public Version Date
March 07, 2022
Public Version Number
1
DI Record Publish Date
February 26, 2022
Package DI Number
50884908139353
Quantity per Package
5
Contains DI Package
30884908139359
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 2560 |