Brand Name | CADD |
Type of Device | SET, ADMINISTRATION, INTRAVASCULAR |
Manufacturer (Section D) |
SMITHS MEDICAL ASD, INC. |
6000 nathan lane north |
minneapolis MN 55442 |
|
MDR Report Key | 11205359 |
MDR Text Key | 227918351 |
Report Number | 3012307300-2021-00605 |
Device Sequence Number | 1 |
Product Code |
FPA
|
UDI-Device Identifier | 15019517161960 |
UDI-Public | 15019517161960 |
Combination Product (y/n) | N |
PMA/PMN Number | K031361 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
foreign,user facility |
Type of Report
| Initial,Followup |
Report Date |
05/28/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 01/20/2021 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
No Information
|
Device Model Number | 21-7363-24 |
Device Catalogue Number | 21-7363-24 |
Device Lot Number | 4025977 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 01/05/2021 |
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 05/01/2021 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
|
|