MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2007-03-06 for IRIX 70 * manufactured by Trophy Radioligie.
[628997]
Irix scissor arm broke at knuckle.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8020825-2007-00004 |
MDR Report Key | 845766 |
Report Source | 05 |
Date Received | 2007-03-06 |
Date of Report | 2007-03-02 |
Date of Event | 2007-02-19 |
Device Manufacturer Date | 1995-03-01 |
Date Added to Maude | 2007-05-10 |
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 | 0 |
Manufacturer Contact | LINDA SPITZER |
Manufacturer Street | 1765 THE EXCHANGE |
Manufacturer City | ATLANTA GA 30339 |
Manufacturer Country | US |
Manufacturer Postal | 30339 |
Manufacturer Phone | 7702263518 |
Manufacturer G1 | TROPHY RADIOLIGIE |
Manufacturer Street | 4 RUE F. PELLOUTIE MARNE LA VALLEE |
Manufacturer City | CROISSY-BEAUBOURG 77437 |
Manufacturer Country | * |
Manufacturer Postal Code | 77437 |
Single Use | 3 |
Remedial Action | NO |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | IRIX 70 |
Generic Name | DENTAL X-RAY SYSTEM |
Product Code | EAP |
Date Received | 2007-03-06 |
Model Number | * |
Catalog Number | * |
Lot Number | * |
ID Number | * |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 832859 |
Manufacturer | TROPHY RADIOLIGIE |
Manufacturer Address | 4 RUE F. PELLOUTIER * * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2007-03-06 |