Duns Number:038000253
Device Description: 5F PLASTIC DIGNITY® MID-SIZED CT PORT W/SILICONE FILLED SUTURE HOLES W/ATTACHABLE ChronoFl 5F PLASTIC DIGNITY® MID-SIZED CT PORT W/SILICONE FILLED SUTURE HOLES W/ATTACHABLE ChronoFlex® POLYURETHANE CATHETER
Catalog Number
MRDP50AMS
Brand Name
DIGNITY®
Version/Model Number
MRDP50AMS
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 17, 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
2d46f6d4-31d8-425b-bbbd-297a88d978ea
Public Version Date
September 15, 2020
Public Version Number
2
DI Record Publish Date
November 28, 2019
Package DI Number
50884908149734
Quantity per Package
5
Contains DI Package
00884908149739
Package Discontinue Date
July 17, 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 |