OUTBACK RE-ENTRY CATHETER Adverse Event — Injury (MDR 9616099-2008-00348)
OUTBACK RE-ENTRY CATHETER Adverse Event — Injury (MDR 9616099-2008-00348) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: OUTBACK RE-ENTRY CATHETER; Generic name: CTO CATHETER SYSTEMS (DQY); Manufacturer: CORDIS DE MEXICO.
| Device | OUTBACK RE-ENTRY CATHETER |
|---|---|
| Generic name | CTO CATHETER SYSTEMS (DQY) |
| Manufacturer | CORDIS DE MEXICO |
| Report number | 9616099-2008-00348 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Health Professional, Company representation |
| Narrative | THIS PRODUCT IS AVAILABLE; HOWEVER, IT HAS NOT BEEN RECEIVED FOR ANALYSIS. ADD'L INFO WILL BE PROVIDED WITHIN 30 DAYS OF RECEIPT. |
| Source | openFDA MAUDE (device adverse events) |
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