PERIFIX Adverse Event — Injury (MDR 9610825-2020-00096)
PERIFIX Adverse Event — Injury (MDR 9610825-2020-00096) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PERIFIX; Generic name: CATHETER, CONDUCTION, ANESTHETIC; Manufacturer: B. BRAUN MELSUNGEN AG.
| Device | PERIFIX |
|---|---|
| Generic name | CATHETER, CONDUCTION, ANESTHETIC |
| Manufacturer | B. BRAUN MELSUNGEN AG |
| Report number | 9610825-2020-00096 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN MELSUNGEN AG INTERNAL REPORT # (B)(4). WE RECEIVED 6 PICTURES OF A PERIFIX CATHETER AND ONE PICTURE OF THE PRIMARY PACKAGING, NO SAMPLE. THE PICTURES SHOW A PERIFIX CATHETER WERE THE CATHETER TIP IS MISSING (APPROX. 10 - 20 MM FROM THE TIP). BASED ON THE PICTURES THE SURFACE OF THE DEMOLITION SITE IS NOT CLEARLY VISIBLE. IT CAN ONLY BE SEEN THAT THE CATH |
| Source | openFDA MAUDE (device adverse events) |
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