Duns Number:038000253
Device Description: 15.5F X 28CM Titan HD FULL SET (CUFF 23CM FROM TIP)
Catalog Number
RMS29502
Brand Name
Titan HD
Version/Model Number
RMS29502
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 28, 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
95ed9624-8ff5-4e68-9590-8e1d53c068ae
Public Version Date
October 04, 2021
Public Version Number
3
DI Record Publish Date
November 26, 2020
Package DI Number
50884908158149
Quantity per Package
5
Contains DI Package
00884908158144
Package Discontinue Date
September 28, 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 |