MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-30 for 17G WALLACE OOCYTE RCVRY ONS1733LL manufactured by Coopersurgical, Inc..
Report Number | 1216677-2019-00270 |
MDR Report Key | 9136062 |
Date Received | 2019-09-30 |
Date of Report | 2019-09-30 |
Date of Event | 2019-09-13 |
Date Mfgr Received | 2019-09-18 |
Device Manufacturer Date | 2018-11-24 |
Date Added to Maude | 2019-09-30 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. PETER NIZIOLEK |
Manufacturer Street | 50 CORPORATE DRIVE |
Manufacturer City | TRUMBULL CT 06611 |
Manufacturer Country | US |
Manufacturer Postal | 06611 |
Manufacturer Phone | 2036015200 |
Manufacturer G1 | COOPERSURGICAL, INC. |
Manufacturer Street | 95 CORPORATE DRIVE |
Manufacturer City | TRUMBULL CT 06611 |
Manufacturer Country | US |
Manufacturer Postal Code | 06611 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | 17G WALLACE OOCYTE RCVRY |
Generic Name | 17G WALLACE OOCYTE RCVRY |
Product Code | MQE |
Date Received | 2019-09-30 |
Model Number | ONS1733LL |
Catalog Number | ONS1733LL |
Lot Number | N/A |
Device Availability | N |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOPERSURGICAL, INC. |
Manufacturer Address | 95 CORPORATE DRIVE TRUMBULL CT 06611 US 06611 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-09-30 |