Duns Number:961027315
Device Description: STR 7 IN SILASTIC TUBING KIT
Catalog Number
SID21ACUHD
Brand Name
CARDINAL HEALTH
Version/Model Number
SID21ACUHD
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
FEG
Product Code Name
TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION
Public Device Record Key
ea90f15b-4ced-4a72-8d93-765432c47df8
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
October 05, 2016
Package DI Number
50885425859861
Quantity per Package
50
Contains DI Package
10885425859863
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 |