Duns Number:961027315
Device Description: Surgical Drain Perforated/Round 19Fr Silicone Center Perforation
Catalog Number
SU130-1327
Brand Name
JACKSON-PRATT
Version/Model Number
SU130-1327
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
-
Product Code
GBX
Product Code Name
CATHETER, IRRIGATION
Public Device Record Key
f9ee38a0-4142-4dc9-b745-fb28a713b816
Public Version Date
March 08, 2022
Public Version Number
2
DI Record Publish Date
December 21, 2018
Package DI Number
50885380039865
Quantity per Package
8
Contains DI Package
20885380039864
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |