MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-12-05 for MANUAL SNAP WRENCH 9095.10.110 manufactured by Limacorporate S.p.a..
Report Number | 3008021110-2019-00144 |
MDR Report Key | 9415904 |
Report Source | OTHER |
Date Received | 2019-12-05 |
Date of Event | 2019-11-26 |
Date Added to Maude | 2019-12-05 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Country | IT |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MANUAL SNAP WRENCH |
Generic Name | MANUAL SNAP WRENCH |
Product Code | HXC |
Date Received | 2019-12-05 |
Model Number | 9095.10.110 |
Catalog Number | 9095.10.110 |
Lot Number | 11H5257 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | LIMACORPORATE S.P.A. |
Manufacturer Address | VIA NAZIONALE 52 VILLANOVA DI SAN DANIELE, 33038 IT 33038 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-05 |