MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-20 for INNER SHEATH, FOR 26 FR. OUTER SHEATH A22040A manufactured by Olympus Winter & Ibe Gmbh.
| Report Number | 2951238-2020-00344 |
| MDR Report Key | 9732720 |
| Date Received | 2020-02-20 |
| Date of Report | 2020-02-20 |
| Date Facility Aware | 2020-01-21 |
| Report Date | 2020-01-22 |
| Date Reported to Mfgr | 2020-01-22 |
| Date Added to Maude | 2020-02-20 |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | INNER SHEATH, FOR 26 FR. OUTER SHEATH |
| Generic Name | RESECTOSCOPE SHEATH |
| Product Code | HIH |
| Date Received | 2020-02-20 |
| Returned To Mfg | 2020-02-18 |
| Model Number | A22040A |
| Catalog Number | A22040A |
| Lot Number | 18YW-0405 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OLYMPUS WINTER & IBE GMBH |
| Manufacturer Address | KUEHNSTRASSE 61 HAMBURG 22045 GM 22045 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-02-20 |