Duns Number:967358115
Device Description: DRYSEAL LUBRICIOUS 22F Hydrophilic Coating
Catalog Number
DSL2228
Brand Name
GORE DRYSEAL Sheath
Version/Model Number
DSL2228
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
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
K121234
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
da0fbcbe-af94-4504-9c4e-1753fc5a3d23
Public Version Date
February 28, 2020
Public Version Number
5
DI Record Publish Date
February 13, 2017
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. | 561 |
3 | A medical device with high risk that requires premarket approval | 623 |