Duns Number:038000253
Device Description: 16F X 24CM PRE-CURVED SPLIT CATH® III CATHETER ONLY (CUFF 19CM FROM TIP)
Catalog Number
-
Brand Name
SPLIT CATH® III
Version/Model Number
AAC23617
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 25, 2021
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
MSD
Product Code Name
Catheter, hemodialysis, implanted
Public Device Record Key
3b2ac241-9099-4a0b-8f24-9ac719dffbd2
Public Version Date
June 22, 2021
Public Version Number
6
DI Record Publish Date
April 29, 2016
Package DI Number
50884908001018
Quantity per Package
10
Contains DI Package
00884908001013
Package Discontinue Date
March 25, 2021
Package Status
Not 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 |