Brand Name | CUROS¿ |
Type of Device | PAD, ALCOHOL, DEVICE DISINFECTANT |
Manufacturer (Section D) |
3M COMPANY |
3m center, 2510 conway ave. |
bldg. 275-5w-06 |
st. paul MN 55144 |
|
MDR Report Key | 8939408 |
MDR Text Key | 155843909 |
Report Number | 8939408 |
Device Sequence Number | 1 |
Product Code |
LKB
|
Combination Product (y/n) | N |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
User Facility
|
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
08/14/2019,08/12/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 08/14/2019 |
Event Location |
Hospital
|
Date Report to Manufacturer | 08/28/2019 |
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 08/28/2019 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
|
|