MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-05-22 for DIRECTINJECT ON DEMAND HA CEMENT 79-45905 manufactured by Stryker Leibinger Freiburg.
[145787823]
The device is not available for evaluation. If additional information is received it will be reported on a supplemental report. Device evaluated by mfr: device is implanted in patient.
Patient Sequence No: 1, Text Type: N, H10
[145787824]
It was reported through a company representative that an infection occurred with a patient after a procedure. The procedure was completed successfully without a delay. There are no additional details available at this time, and device "relativity"/involvement is unknown.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0008010177-2019-00020 |
| MDR Report Key | 8632041 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2019-05-22 |
| Date of Report | 2019-08-01 |
| Date of Event | 2019-05-08 |
| Date Mfgr Received | 2019-05-08 |
| Date Added to Maude | 2019-05-22 |
| 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 | MR. GREGORY GOHL |
| Manufacturer Street | BOETZINGERSTR. 41 |
| Manufacturer City | FREIBURG D-79111 |
| Manufacturer Postal | D-79111 |
| Manufacturer Phone | 76145120 |
| Manufacturer G1 | STRYKER LEIBINGER FREIBURG |
| Manufacturer Street | BOETZINGERSTR. 41 |
| Manufacturer City | FREIBURG D-79111 |
| Manufacturer Postal Code | D-79111 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DIRECTINJECT ON DEMAND HA CEMENT |
| Generic Name | IMPLANT |
| Product Code | GXP |
| Date Received | 2019-05-22 |
| Catalog Number | 79-45905 |
| Lot Number | UNK |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER LEIBINGER FREIBURG |
| Manufacturer Address | BOETZINGERSTR. 41 FREIBURG D-79111 D-79111 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-05-22 |