Brand Name | JUVEDERM ULTRA XC/LIDO (VOLUME UNKNOWN) |
Type of Device | IMPLANT, DERMAL, FOR AESTHETIC USE |
Manufacturer (Section D) |
ALLERGAN (PRINGY) |
route de promery |
zone artisanale de pre-mairy |
pringy |
|
Manufacturer (Section G) |
ALLERGAN (PRINGY) |
route de promery |
zone artisanale de pre-mairy |
pringy |
|
Manufacturer Contact |
chris
sprague
|
12331-a riata trace parkway |
building 3 |
austin, TX 78727
|
8479375615
|
|
MDR Report Key | 14030677 |
MDR Text Key | 291239614 |
Report Number | 3005113652-2022-00217 |
Device Sequence Number | 1 |
Product Code |
LMH
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P050047 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Consumer,Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
04/06/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 04/06/2022 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Catalogue Number | UNK JUVEDERM ULTRA XC/LIDO |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 03/29/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Sex | Female |