MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2006-03-24 for MAQUET 1132.11B2 manufactured by Maquet Gmbh & Co. Kg.
| Report Number | 8010652-2006-00002 |
| MDR Report Key | 692916 |
| Report Source | 05,06 |
| Date Received | 2006-03-24 |
| Date of Report | 2006-02-24 |
| Date of Event | 2006-01-11 |
| Date Mfgr Received | 2006-02-24 |
| Date Added to Maude | 2006-03-30 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | LORRY CORDARO |
| Manufacturer Street | 1777 E HENRIETTA RD |
| Manufacturer City | ROCHESTER NY 146233133 |
| Manufacturer Country | US |
| Manufacturer Postal | 146233133 |
| Manufacturer Phone | 5857451400 |
| Manufacturer G1 | MAQUET GMBH & CO. KG |
| Manufacturer Street | KEHLER STRASSE 31 |
| Manufacturer City | RASTATT 76437 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 76437 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MAQUET |
| Generic Name | OPERATING TABLE |
| Product Code | FSE |
| Date Received | 2006-03-24 |
| Model Number | 1132.11B2 |
| Operator | HEALTH PROFESSIONAL |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 668729 |
| Manufacturer | MAQUET GMBH & CO. KG |
| Manufacturer Address | KEHLER STRASSE 31 RASTATT GM 76437 |
| Baseline Brand Name | MAQUET |
| Baseline Generic Name | OPERATING TABLE |
| Baseline Model No | 1132.11B2 |
| Baseline Catalog No | * |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-03-24 |