| Brand Name | React catheter |
| Common Device Name | CATHETER, PERCUTANEOUS, NEUROVASCULATURE |
| 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 |
|
justin
ellis
|
| 9775 toledo way |
| irvine, CA 92618
|
|
+1(763)526-5677
|
|
| MDR Report Key | 50715909 |
| Report Number | 2029214-2026-01816 |
| Device Sequence Number | 10611675 |
| Product Code |
QJP
|
| UDI-Device Identifier | 00847536031784 |
| UDI-Public | (01)00847536031784(17)280518(10)D115437 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | CH |
| PMA/510(K) Number | K182097 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional,Company Representative |
| Initial Reporter Occupation |
Physician
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/10/2026 |
| 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
|
| Operator of Device |
Health Professional
|
| Device Model Number | REACT-71 |
| Device Catalogue Number | REACT-71 |
| Device Lot Number | D115437 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 09/08/2026 |
| Initial Report FDA Received Date | 09/10/2026 |
| Date Device Manufactured | 05/27/2026 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Patient Sequence Number | 1 |
| Patient Age | 67 YR |
| Patient Sex | Male |
| Patient Weight | 157 LB |
|
|