MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-03-27 for SOFIA 5F 115 CM STR DA5115ST manufactured by Microvention, Inc.
| Report Number | 2032493-2020-00077 |
| MDR Report Key | 9892279 |
| Report Source | DISTRIBUTOR,FOREIGN,HEALTH PR |
| Date Received | 2020-03-27 |
| Date of Report | 2020-02-27 |
| Date of Event | 2020-02-21 |
| Date Mfgr Received | 2020-02-27 |
| Device Manufacturer Date | 2019-09-02 |
| Date Added to Maude | 2020-03-27 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. EVA MANUS |
| Manufacturer Street | 35 ENTERPRISE DRIVE |
| Manufacturer City | ALISO VIEJO, CA |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SOFIA 5F 115 CM STR |
| Generic Name | PERCUTANEOUS CATHETER |
| Product Code | DQY |
| Date Received | 2020-03-27 |
| Returned To Mfg | 2020-03-11 |
| Model Number | DA5115ST |
| Catalog Number | DA5115ST |
| Lot Number | 19090257H |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MICROVENTION, INC |
| Manufacturer Address | 35 ENTERPRISE DRIVE ALISO VIEJO, CA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-27 |