MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-12-21 for HHP SCANNER * manufactured by *.
Report Number | 2250051-2004-50515 |
MDR Report Key | 959373 |
Date Received | 2004-12-21 |
Date of Report | 2004-12-21 |
Date of Event | 2004-11-22 |
Date Added to Maude | 2007-12-07 |
Event Key | 0 |
Report Source Code | Distributor report |
Manufacturer Link | N |
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 | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HHP SCANNER |
Generic Name | BARCODE SCANNER |
Product Code | LRH |
Date Received | 2004-12-21 |
Model Number | * |
Catalog Number | * |
Lot Number | A4070567-D07 |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | * |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 929611 |
Manufacturer | * |
Manufacturer Address | * * * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2004-12-21 |