Brand Name | ARCTIC SUN® 5000 |
Type of Device | ARCTIC SUN DEVICE |
Manufacturer (Section D) |
MEDIVANCE, INC. ¿ 1725056 |
321 s taylor ave |
suite 200 |
louisville 80027 |
|
Manufacturer (Section G) |
MEDIVANCE, INC. ¿ 1725056 |
321 s taylor ave |
suite 200 |
louisville 80027 |
|
Manufacturer Contact |
yonic
anderson
|
8195 industrial blvd |
covington 30014
|
7707846100
|
|
MDR Report Key | 13129708 |
MDR Text Key | 287017999 |
Report Number | 1018233-2021-08662 |
Device Sequence Number | 1 |
Product Code |
DWJ
|
Combination Product (y/n) | N |
Reporter Country Code | UK |
PMA/PMN Number | K161602 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Health Professional,User Facility |
Reporter Occupation |
|
Type of Report
| Initial |
Report Date |
12/23/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/31/2021 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
|
Device Catalogue Number | 5000-01-02 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 12/10/2021 |
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 12/21/2021 |
Was Device Evaluated by Manufacturer? |
No
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Treatment Data |
Date Received: 12/31/2021 Patient Sequence Number: 1 |
|
|