Duns Number:038000253
Device Description: 8F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLE ChronoFlex® POLYURETHANE CATHETER W/5F MICRO-STI 8F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLE ChronoFlex® POLYURETHANE CATHETER W/5F MICRO-STICK® INTRODUCER SET
Catalog Number
MIPP80AFS
Brand Name
PRO-FUSE®
Version/Model Number
MIPP80AFS
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 13, 2021
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
LJT
Product Code Name
PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR
Public Device Record Key
cfea3ed5-b170-455f-a738-31109df033a7
Public Version Date
September 17, 2021
Public Version Number
2
DI Record Publish Date
November 26, 2019
Package DI Number
50884908149697
Quantity per Package
5
Contains DI Package
00884908149692
Package Discontinue Date
July 13, 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 |