MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-25 for MAQUET EDI CATHETER REF 6685775, 6/49 FR/CM manufactured by Maquet Medical Systems, Usa.
| Report Number | MW5087601 |
| MDR Report Key | 8735018 |
| Date Received | 2019-06-25 |
| Date of Report | 2019-06-21 |
| Date of Event | 2019-06-20 |
| Date Added to Maude | 2019-06-26 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| 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 | MAQUET EDI CATHETER REF 6685775, 6/49 FR/CM |
| Generic Name | GASTROINTESTINAL, TUBES WITH ENTERAL SPECIFIC CONNECTORS |
| Product Code | PIF |
| Date Received | 2019-06-25 |
| Returned To Mfg | 2019-06-20 |
| Model Number | MAQUET EDI CATHETER REF 6685775 |
| Catalog Number | MAQUET EDI CATHETER REF 668577 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MAQUET MEDICAL SYSTEMS, USA |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-06-25 |