MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-11-06 for STRYKER MANDIBLE SET DRILL GUID TROCARE TIP UNKNOWN manufactured by Stryker Leibinger Gmbh & Co. Kg.
| Report Number | MW5090942 |
| MDR Report Key | 9291103 |
| Date Received | 2019-11-06 |
| Date of Report | 2019-11-01 |
| Date of Event | 2019-10-30 |
| Date Added to Maude | 2019-11-07 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | STRYKER MANDIBLE SET DRILL GUID TROCARE TIP |
| Generic Name | EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR |
| Product Code | MQN |
| Date Received | 2019-11-06 |
| Model Number | UNKNOWN |
| Lot Number | UNKNOWN |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER LEIBINGER GMBH & CO. KG |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-11-06 |