Duns Number:038000253
Device Description: 5F PLASTIC PRO-FUSE® LOW PROFILE CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER W/ 5F PLASTIC PRO-FUSE® LOW PROFILE CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER W/5F MICRO-STICK® INTRODUCER SET
Catalog Number
MIPP50ALN
Brand Name
PRO-FUSE®
Version/Model Number
MIPP50ALN
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 03, 2020
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
96c895ea-53eb-4dd1-be2e-f94cd8b0371e
Public Version Date
October 06, 2020
Public Version Number
2
DI Record Publish Date
November 26, 2019
Package DI Number
50884908149611
Quantity per Package
5
Contains DI Package
00884908149616
Package Discontinue Date
August 03, 2020
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 |