Duns Number:961027315
Device Description: JP 3-SPRING RES W/19FR PVC DRAIN/TR
Catalog Number
SU130-404D
Brand Name
CARDINAL HEALTH
Version/Model Number
SU130-404D
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
May 30, 2024
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GCY
Product Code Name
APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED
Public Device Record Key
dc883838-dff0-4bdb-8663-ada1e7a74fe2
Public Version Date
February 19, 2021
Public Version Number
4
DI Record Publish Date
May 01, 2018
Package DI Number
50885380113121
Quantity per Package
1
Contains DI Package
20885380113120
Package Discontinue Date
May 30, 2024
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 |