Brand Name | WEBSTER CS |
Type of Device | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
Manufacturer (Section D) |
BIOSENSE WEBSTER INC |
31 technology drive, suite 200 |
irvine CA 92618 |
|
MDR Report Key | 14521739 |
MDR Text Key | 292801517 |
Report Number | 14521739 |
Device Sequence Number | 1 |
Product Code |
DRF
|
Combination Product (y/n) | N |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
User Facility
|
Reporter Occupation |
Risk Manager
|
Type of Report
| Initial |
Report Date |
05/18/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | BD710FJ282RTS |
Device Catalogue Number | BD710FJ282RTS |
Device Lot Number | 30740924M |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
No
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 05/18/2022 |
Event Location |
Hospital
|
Date Report to Manufacturer | 05/27/2022 |
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 05/27/2022 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Age | 25915 DA |
Patient Sex | Male |
Patient Weight | 86 KG |
Patient Race | White |
|
|