Brand Name | ONYX |
Type of Device | AGENT, INJECTABLE, EMBOLIC |
Manufacturer (Section D) |
MICRO THERAPEUTICS, INC. DBA EV3 |
9775 toledo way |
irvine CA 92618 |
|
Manufacturer (Section G) |
MICRO THERAPEUTICS, INC. DBA EV3 |
9775 toledo way |
|
irvine CA 92618 |
|
Manufacturer Contact |
glen
belmer
|
9775 toledo way |
irvine, CA 92618
|
6122713209
|
|
MDR Report Key | 13935066 |
MDR Text Key | 288132771 |
Report Number | 2029214-2022-00507 |
Device Sequence Number | 1 |
Product Code |
MFE
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
03/28/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | UNK-NV-ONYX |
Device Catalogue Number | UNK-NV-ONYX |
Device Lot Number | UNKNOWN |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
03/04/2022 |
Initial Date FDA Received | 03/29/2022 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|