MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-06-18 for RESECTION SHEATH, 24 FR. A22041A manufactured by Olympus Winter & Ibe Gmbh.
Report Number | 9610773-2019-00071 |
MDR Report Key | 8706819 |
Report Source | COMPANY REPRESENTATIVE,DISTRI |
Date Received | 2019-06-18 |
Date of Report | 2019-06-25 |
Date Mfgr Received | 2019-06-21 |
Device Manufacturer Date | 2019-01-01 |
Date Added to Maude | 2019-06-18 |
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. DANIEL WLADOW |
Manufacturer Street | KUEHNSTRASSE 61 |
Manufacturer City | HAMBURG 22045 |
Manufacturer Country | GM |
Manufacturer Postal | 22045 |
Manufacturer Phone | 4940669662 |
Manufacturer G1 | OLYMPUS WINTER & IBE GMBH |
Manufacturer Street | KUEHNSTRASSE 61 |
Manufacturer City | HAMBURG |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | RESECTION SHEATH, 24 FR. |
Generic Name | RESECTION SHEATHS, IRRIGATION RINGS, CYSTOSCOPE SHEATHS, HYSTEROSCOPE SHEATHS |
Product Code | FJL |
Date Received | 2019-06-18 |
Returned To Mfg | 2019-06-18 |
Model Number | A22041A |
Catalog Number | A22041A |
Lot Number | 191W |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | OLYMPUS WINTER & IBE GMBH |
Manufacturer Address | KUEHNSTRASSE 61 HAMBURG US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-18 |